Pharmacovigilance Jobs

ClinChoice Hiring Senior Associate MICC – Pharmacovigilance & Medical Information

March 15, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now ClinChoice Senior Associate MICC Jobs in Bangalore – Pharmacovigilance & Medical Information Careers ClinChoice is hiring Senior Associate – MICC (Medical Information Contact Center) professionals for its global pharmacovigilance and medical information operations team in Bangalore, India. This full-time opportunity is designed for candidates with Pharmacy or Life Sciences backgrounds and 4+ years of experience in medical information handling, pharmacovigilance support, or healthcare contact center environments. The role focuses on handling medical inquiries, adverse event reports, product complaints, and drug safety communication from healthcare professionals and consumers. Professionals with experience in pharmacovigilance call handling, medical information services, and adverse event monitoring will find this position highly aligned with career growth in the global clinical research and drug safety industry. Candidates will work with international pharmaceutical clients supporting patient safety monitoring, product complaint handling, and medical information management while ensuring compliance with global regulatory guidelines. Company Overview ClinChoice is a global clinical research organization (CRO) that partners with leading pharmaceutical, biotechnology, and medical device companies to support clinical development and regulatory compliance. Founded in 1995, the organization provides specialized services in clinical operations, biometrics, pharmacovigilance, regulatory affairs, medical affairs, and toxicology. ClinChoice supports healthcare innovators across the entire product lifecycle, from early clinical trials to post-marketing safety monitoring. The company leverages data-driven insights and advanced clinical analytics to accelerate drug development and enhance patient safety worldwide. With delivery centers located in the United States, United Kingdom, Mexico, Armenia, China, Japan, India, and the Philippines, ClinChoice provides global regulatory and clinical support services to pharmaceutical sponsors operating in multiple markets. By joining ClinChoice, professionals gain exposure to international clinical development programs, global pharmacovigilance frameworks, and cutting-edge healthcare technologies that support the development and monitoring of safe and effective medicines. Job Role and Responsibilities The Senior Associate – MICC plays an important role in handling medical information requests, pharmacovigilance case intake, and product complaint management within the organization’s Medical Information Contact Center. Professionals in this role interact directly with healthcare professionals and consumers to capture safety information, resolve product-related concerns, and ensure regulatory reporting compliance. Medical Information and Customer Support • Handle inbound and outbound calls and emails related to medical inquiries, adverse events, and product complaints • Provide accurate product and service information to healthcare professionals and consumers • Respond to web-based medical inquiries regarding safety and effective use of marketed pharmaceutical products • Follow up with healthcare professionals and patients regarding medical information queries • Maintain high standards of customer service while addressing medical or product-related concerns Pharmacovigilance Case Intake • Identify and document Adverse Events (AEs) and Product Complaints (PCs) reported by healthcare professionals or consumers • Capture safety information related to medication errors, device complaints, and special safety scenarios • Process both spontaneous and solicited pharmacovigilance reports • Generate follow-up requests for missing information related to safety cases • Prepare documentation required for adverse event monitoring forms Product Complaint Management • Record product complaints received via calls, emails, or web portals • Investigate discrepancies related to product complaints • Generate and send follow-up letters for product complaint cases • Escalate safety or product-related issues to relevant internal teams Medical Documentation and Data Management • Document all call information and case details according to medical information standard operating procedures • Maintain accurate call logs and documentation records • Update medical information templates and follow-up documentation as required • Ensure documentation meets regulatory and company compliance standards Regulatory Compliance and Quality Assurance • Maintain working knowledge of Global Pharmacovigilance Practices (GVP) and related modules • Ensure compliance with global regulatory guidelines related to pharmacovigilance and drug safety reporting • Follow client-specific standard operating procedures and project workflows • Support medical reviewers by providing accurate case documentation Customer Interaction and Issue Resolution • Research and identify appropriate responses to customer complaints • Route calls and queries to appropriate internal departments when required • Provide timely resolution of inquiries while maintaining compliance with regulatory standards • Maintain professionalism and empathy when interacting with patients and healthcare professionals Through these responsibilities, the Senior Associate contributes to ensuring accurate drug safety monitoring, effective medical communication, and regulatory compliance for marketed pharmaceutical products. Eligibility and Qualifications Candidates interested in applying for the Senior Associate – MICC role at ClinChoice should possess a strong healthcare or life sciences educational background along with relevant professional experience. Educational Qualification Graduates in pharmacy or life sciences. Relevant educational backgrounds include: B.Pharm, M.Pharm, BSc Life Sciences, BSc Biotechnology, BSc Microbiology, BSc Biochemistry, MSc Biotechnology, MSc Microbiology, MSc Biochemistry, MSc Pharmacology, MSc Life Sciences. Experience • Minimum 3–5 years of experience in a US or UK healthcare call center environment • Experience in pharmacovigilance case intake, medical information handling, or drug safety communication is preferred Technical Skills • Knowledge of pharmacovigilance safety reporting and adverse event documentation • Understanding of Global Pharmacovigilance Practices (GVP) • Experience handling product complaints and medical information queries • Proficiency in Microsoft Office applications and documentation tools • Ability to manage safety case documentation and follow-up communications Professional Skills • Excellent verbal and written communication skills • Strong customer service and interpersonal skills • Ability to handle multiple tasks in a fast-paced environment • Strong attention to detail and documentation accuracy • Ability to manage stressful situations professionally • Strong listening and problem-solving abilities • Flexibility to work rotational shifts including weekends Professionals with experience in medical information services, pharmacovigilance call centers, drug safety communication, and healthcare customer support will find this role highly suitable for advancing careers in global pharmaceutical safety operations. Location and Salary Location: Bangalore, Karnataka, India Work Type: Full-time position within medical information contact center operations Work Environment: Office-based role with rotational shifts Salary: Competitive salary package aligned with CRO pharmacovigilance and medical information industry standards. Employees at ClinChoice gain exposure to global pharmaceutical programs, regulatory drug safety frameworks, and international clinical development operations. Application Process Candidates interested in applying for the Senior Associate – MICC position can submit their applications through the official ClinChoice careers portal. Apply Here: https://job-boards.eu.greenhouse.io/clinchoice/jobs/4787022101 Applicants are encouraged to apply early as pharmacovigilance and medical information roles within CRO organizations typically receive high volumes of applications. Frequently Asked Questions What does a Medical Information Contact Center Associate do? A Medical Information Contact Center Associate responds to medical inquiries, records adverse events, manages product complaints, and ensures accurate pharmacovigilance documentation while supporting healthcare professionals and patients. Who can apply for this ClinChoice job? Candidates with pharmacy or life sciences degrees and several years of experience in healthcare call centers or pharmacovigilance environments can apply. What is MICC in pharmacovigilance? MICC stands for Medical Information Contact Center. It is a specialized department that manages medical inquiries, adverse event reporting, and product complaint communication for pharmaceutical companies. Is pharmacovigilance knowledge required? Yes. Understanding of pharmacovigilance regulations, adverse event reporting, and Global Pharmacovigilance Practices is beneficial for this role. Where is the job located? The role is based in Bangalore, India, within ClinChoice’s medical information and pharmacovigilance operations team. Job Summary Category Details Company ClinChoice Vacancies Senior Associate – MICC Required Education B.Pharm, M.Pharm, BSc Life Sciences, BSc Biotechnology, BSc Microbiology, BSc Biochemistry, MSc Biotechnology, MSc Microbiology, MSc Biochemistry, MSc Pharmacology Experience 3–5 years Healthcare Call Center / Pharmacovigilance Experience [...] Read more...

Syneos Health Recruiting Safety & Pharmacovigilance Coordinator

March 14, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Syneos Health Safety & Pharmacovigilance Coordinator Jobs in Gurgaon – B.Pharm / PharmD Drug Safety Careers Syneos Health is currently hiring Safety & Pharmacovigilance Coordinator professionals for its drug safety and pharmacovigilance operations team in Gurgaon, Haryana, India. This opportunity is ideal for healthcare graduates such as B.Pharm, M.Pharm, PharmD, or BDS who have at least 1 year of experience in pharmacovigilance, clinical trial safety data entry, or literature case processing. The position focuses on Individual Case Safety Report (ICSR) processing, pharmacovigilance data entry, clinical trial safety documentation, and regulatory safety support within global drug development programs. Candidates with experience in clinical trial safety cases, literature safety cases, and safety database management will find this role highly aligned with career growth in the clinical research and pharmaceutical drug safety industry. This full‑time role is based on‑site in Gurgaon, Haryana, and offers the opportunity to work with global clinical development teams supporting pharmaceutical sponsors and regulatory safety operations worldwide. Company Overview Syneos Health is a leading fully integrated biopharmaceutical solutions organization that helps pharmaceutical, biotechnology, and healthcare companies accelerate the development and commercialization of innovative therapies. The company combines clinical development, medical affairs, and commercial capabilities to support the entire lifecycle of medicines. Operating across 110 countries with more than 29,000 employees, Syneos Health plays a major role in global drug development and clinical research operations. Over the past several years, the company has contributed to 94% of all FDA‑approved novel medicines and 95% of EMA‑authorized products, demonstrating its strong presence in the pharmaceutical research ecosystem. The organization’s clinical development model focuses on placing both the patient and the sponsor at the center of drug development, ensuring faster, efficient delivery of life‑saving treatments. Employees working at Syneos Health benefit from a collaborative environment that emphasizes professional growth, technical training, and global exposure in clinical research and pharmacovigilance. Job Role and Responsibilities The Safety & Pharmacovigilance Coordinator supports global pharmacovigilance operations by assisting with the collection, processing, and documentation of safety information related to pharmaceutical products. The role focuses heavily on accurate data handling, case tracking, and compliance with global safety regulations. Pharmacovigilance Case Processing • Monitor incoming safety information from multiple sources and route it to appropriate project teams • Assist with the preparation and processing of Individual Case Safety Reports (ICSRs) • Perform accurate data entry of safety cases into pharmacovigilance databases • Maintain proper documentation of safety cases in accordance with sponsor requirements • Track safety cases and maintain case logs according to project guidelines Safety Documentation and Data Handling • Record and maintain ICSR documentation within safety tracking systems • Redact patient‑identifying information from safety documents to comply with data protection guidelines • Ensure compliance with ICH‑GCP, GVP, and regulatory pharmacovigilance standards • Create and maintain case files in both electronic and paper formats • Maintain accurate documentation for audit and inspection readiness Safety Data Entry and Database Management • Perform timely and accurate data entry into pharmacovigilance safety databases • Maintain case tracking and workflow systems for safety reports • Assist in daily workflow reconciliation activities • Ensure safety data is captured according to client‑specific and internal SOP requirements Case Processing Support Activities • Support query follow‑up activities for incomplete or missing case information • Assist in safety submission processes where required • Coordinate translation of source documents when necessary • Support pharmacovigilance teams in processing literature and clinical trial safety cases Compliance and Quality Assurance • Maintain working knowledge of Standard Operating Procedures (SOPs) and Work Instructions (WIs) • Follow global pharmacovigilance regulations and drug safety guidelines • Maintain awareness of ICH guidelines, GCP standards, and GVP modules • Ensure compliance with project‑specific safety management plans and regulatory requirements Through these responsibilities, the Safety & Pharmacovigilance Coordinator contributes to accurate drug safety monitoring and regulatory compliance during clinical trials and post‑marketing surveillance. Eligibility and Qualifications Candidates applying for the Safety & Pharmacovigilance Coordinator role should have educational backgrounds in healthcare or pharmaceutical sciences along with experience in pharmacovigilance operations. Educational Qualification Healthcare professional degree in relevant disciplines. Relevant education backgrounds include: B.Pharm, M.Pharm, PharmD, BDS, Pharmacy, Pharmaceutical Sciences, Clinical Pharmacy, Pharmacology. Experience • Minimum 1 year of experience in pharmacovigilance case processing or safety data entry • Experience working with clinical trial (CT) safety cases or literature safety cases is preferred Technical Skills • Knowledge of pharmacovigilance safety databases and drug safety workflows • Understanding of medical terminology and adverse event reporting • Familiarity with ICH‑GCP guidelines and pharmacovigilance regulations • Experience processing ICSR safety reports • Proficiency in Microsoft Office tools including Word, Excel, and PowerPoint • Familiarity with document management systems such as TeamShare or similar tools Professional Skills • Strong attention to detail and data accuracy • Excellent written and verbal communication skills • Strong organizational and documentation capabilities • Ability to manage multiple tasks in a fast‑paced clinical research environment • Ability to collaborate effectively with global pharmacovigilance teams • Flexibility to work in rotational shifts when required Professionals with experience in drug safety case processing, pharmacovigilance data entry, and clinical trial safety documentation will find this role well aligned with long‑term careers in global CRO organizations. Location and Salary Location: Gurgaon, Haryana, India Work Model: On‑site Work Type: Full‑time role within global pharmacovigilance operations Application Process Candidates interested in applying for the Safety & Pharmacovigilance Coordinator role can submit their applications through the official Syneos Health careers portal. Apply Here: https://syneoshealth.wd12.myworkdayjobs.com/Syneos_Health_External_Site/job/IND-Gurugram/Safety—Pharmacovigilance-Coordinator–1–Year-Experience-in-CT-or-Literature-Data-Entry-_25104873 Applicants are encouraged to apply early since pharmacovigilance roles within global CRO organizations typically receive high application volumes. Frequently Asked Questions What does a Pharmacovigilance Coordinator do? A Pharmacovigilance Coordinator assists with processing safety cases, managing pharmacovigilance databases, documenting adverse events, and supporting regulatory drug safety reporting during clinical trials and post‑marketing monitoring. Who can apply for this Syneos Health role? Candidates with healthcare degrees such as B.Pharm, M.Pharm, PharmD, or BDS with at least one year of pharmacovigilance or safety data entry experience can apply. What is ICSR in pharmacovigilance? ICSR stands for Individual Case Safety Report. It is a detailed report that documents adverse events associated with pharmaceutical products during clinical trials or post‑marketing monitoring. Is clinical trial safety experience required? Yes. Experience working with clinical trial safety cases or literature safety cases is preferred for this role. Where is the job located? The role is located in Gurgaon, Haryana, India, within Syneos Health’s pharmacovigilance operations team. Job Summary Category Details Company Syneos Health Vacancies Safety & Pharmacovigilance Coordinator Required Education B.Pharm, M.Pharm, PharmD, BDS, Pharmacy, Pharmaceutical Sciences, Pharmacology Experience Minimum 1 year Pharmacovigilance / Safety Data Entry [...] Read more...

Accenture Fresher Pharmacovigilance Vacancies Bangalore

March 13, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Accenture Pharmacovigilance New Associate Hiring – Bengaluru Accenture hiring Pharmacovigilance New Associates in Bengaluru. BAMS, BSc Nursing, Life Sciences. Fresher roles. Apply online. Accenture has opened hiring for the role of Pharmacovigilance Services New Associate at its Bengaluru location. This opportunity is ideal for freshers and early-career professionals from life sciences and healthcare backgrounds who are looking to build a long-term career in pharmacovigilance, drug safety, and regulatory compliance. With structured training, global exposure, and standardized safety operations, this role offers a strong entry point into the global drug safety ecosystem. Pharmacovigilance continues to be a high-demand domain due to increasing regulatory scrutiny, post-marketing surveillance requirements, and global clinical development activities. Joining Accenture in a drug safety role places candidates at the intersection of healthcare, data, and regulatory science, contributing directly to patient safety and public health outcomes. Company Overview Accenture is a global professional services organization with deep expertise across digital, cloud, security, and life sciences operations. Operating in more than 120 countries with a workforce of over 790,000 professionals, Accenture supports leading pharmaceutical, biotechnology, and healthcare organizations through technology-enabled services and intelligent operations. In the life sciences domain, Accenture plays a critical role in pharmacovigilance operations, clinical safety, regulatory compliance, and real-world evidence management. The company partners with global pharma clients to ensure timely adverse event reporting, regulatory submissions, and compliance with international safety regulations. Accenture’s strong governance framework, training programs, and global delivery model make it a trusted employer for careers in drug safety and pharmacovigilance. Job Role & Responsibilities As a Pharmacovigilance Services New Associate, you will support end-to-end drug safety operations and contribute to accurate and timely processing of adverse event data in global safety databases. Core Responsibilities Perform intake, triage, and case creation of Individual Case Safety Reports (ICSRs) Identify and process adverse events (AEs), serious adverse events (SAEs), and SUSARs Create and maintain cases in the global safety database as per client SOPs Perform case data entry, quality checks, and follow-up processing Ensure compliance with global regulatory timelines and submission requirements Conduct medical and drug coding using MedDRA and WHO-Drug dictionaries Draft case narratives and reviewer comments as per regulatory standards Perform duplicate checks, case corrections, and case deletions when required Support submission of safety reports through E2B and regulatory gateways Monitor and reconcile client mailboxes and intake sources Additional Responsibilities Assist in audits, inspections, and compliance activities Support pharmacovigilance projects and transition activities Perform document archiving and data validation activities Coordinate with cross-functional and client teams for safety deliverables Translate source documents and narratives when required Eligibility / Qualifications Required Educational Background Candidates must hold one of the following qualifications: Bachelor of Ayurvedic Medicine and Surgery (BAMS), BSc Nursing, Bachelor Degree in Life Sciences Experience Requirement 0 to 1 year of experience in pharmacovigilance or drug safety operations Freshers with strong subject knowledge are eligible Skill Requirements Knowledge of pharmacovigilance and drug safety concepts Understanding of adverse event reporting and case processing Familiarity with medical terminology Exposure to MedDRA and WHO-Drug dictionaries is preferred Basic knowledge of global safety databases is an advantage Proficiency in MS Office applications Strong medical writing and documentation skills Excellent English communication skills (reading, writing, listening, speaking) Location & Salary Job Location Bengaluru, Karnataka Salary Information Salary details are not disclosed and will be offered based on company norms, qualification, and interview performance. Pharmacovigilance roles fall under high-value healthcare analytics and compliance segments due to regulatory responsibility and global demand. Application Process Interested and eligible candidates must apply online through Accenture’s official career portal. Apply Here: https://www.accenture.com/in-en/careers/jobdetails?id=AIOC-S01621688_en&title=Pharmacovigilance+Services+New+Associate Frequently Asked Questions (FAQs) Who can apply for this Accenture pharmacovigilance role? Candidates with BAMS, BSc Nursing, or a bachelor’s degree in Life Sciences are eligible. Is this role suitable for freshers? Yes. Candidates with 0 to 1 year of experience can apply. What skills are required for pharmacovigilance jobs? Knowledge of adverse event reporting, medical terminology, MedDRA coding, and safety databases is preferred. Where is the job location? The position is based in Bengaluru, Karnataka. How can candidates apply? Applications must be submitted through Accenture’s official career portal. Category Details Company Accenture Vacancies Pharmacovigilance New Associate Required Education BAMS, BSc Nursing, Life Sciences Experience 0 to 1 Year [...] Read more...

Fortrea Pharmacovigilance Safety Specialist I

March 13, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Fortrea Clinical Safety Specialist I Jobs in Bangalore – Pharmacovigilance Careers for Pharmacy & Life Sciences Graduates Fortrea is hiring for the position of Specialist I – Clinical Safety in the Clinical Pharmacovigilance and Drug Safety department at its Bangalore location. This opportunity is designed for professionals with educational backgrounds in pharmacy, life sciences, biological sciences, nursing, or medical sciences who are interested in building careers in pharmacovigilance, adverse event case processing, and clinical trial safety monitoring. The position focuses on managing adverse event (AE) and serious adverse event (SAE) reporting activities generated from clinical trials and post‑marketing safety sources. Professionals with 1–2 years of pharmacovigilance experience or relevant pharmaceutical/CRO experience will find this role suitable for advancing their careers in the global drug safety and clinical research industry. This role is based in Bangalore, India, within Fortrea’s clinical safety operations team and offers exposure to global regulatory safety reporting, clinical trial monitoring, and pharmacovigilance database management used across international pharmaceutical programs. Company Overview Fortrea is a global contract research organization (CRO) specializing in clinical development, patient safety monitoring, regulatory support, and data management services for pharmaceutical, biotechnology, and medical device companies. The organization supports drug development across the full clinical lifecycle including clinical trials, pharmacovigilance operations, regulatory submissions, and post‑marketing safety surveillance. By partnering with global pharmaceutical sponsors, Fortrea ensures medicines are developed and monitored according to international regulatory standards. Fortrea’s clinical safety teams play a vital role in monitoring drug safety, managing adverse event reports, and ensuring timely regulatory reporting to health authorities worldwide. The company operates in a highly regulated environment guided by ICH guidelines, Good Clinical Practice (GCP), and global pharmacovigilance regulations. Professionals working at Fortrea gain exposure to multinational clinical trials, global drug safety databases, and regulatory reporting frameworks that support the safe use of medicines worldwide. Job Role and Responsibilities The Specialist I – Clinical Safety supports pharmacovigilance and patient safety operations related to clinical trials and marketed pharmaceutical products. The role focuses on case processing, safety database management, and regulatory reporting activities within global drug safety programs. Adverse Event Case Processing • Receive and process adverse event reports collected from clinical trials or spontaneous post‑marketing sources • Enter safety data into pharmacovigilance databases and tracking systems • Review adverse event cases for completeness, accuracy, and regulatory reporting requirements • Write clear and accurate patient narratives based on safety case information • Code adverse events using MedDRA terminology • Identify missing safety information and initiate follow‑up queries where necessary Regulatory Safety Reporting • Process and submit Serious Adverse Event (SAE) reports within regulatory timelines • Support submission of safety reports to clients, regulatory authorities, ethics committees, investigators, and study partners • Prepare and support submission of Expedited Safety Reports (ESRs) and Periodic Safety Reports (PSRs) • Assist with preparation of safety listings for Periodic Safety Update Reports (PSURs) and Development Safety Update Reports (DSURs) Safety Data Management • Maintain safety tracking systems and pharmacovigilance databases • Perform reconciliation activities with clinical data management teams or sponsors • Maintain project files and central safety documentation records • Ensure documentation readiness for audits and regulatory inspections Signal Detection and Safety Monitoring • Participate in safety signal detection activities and pattern recognition • Support preparation of safety metrics and monthly safety reports • Assist with cumulative safety data reviews required for regulatory reporting Compliance and Quality Management • Follow pharmacovigilance Standard Operating Procedures (SOPs) and Work Instructions • Assist in updating Safety Management Plans and reconciliation procedures • Support audit and inspection readiness activities • Contribute to root cause analysis and CAPA implementation when required Collaboration and Team Support • Participate in project meetings and discussions with clients and internal teams • Provide support and guidance to junior pharmacovigilance staff • Coordinate with cross‑functional teams including data management and regulatory affairs • Ensure high‑quality service delivery for both internal and external stakeholders Through these responsibilities, the Specialist I role contributes to ensuring patient safety, regulatory compliance, and accurate safety monitoring throughout the clinical development process. Eligibility and Qualifications Candidates interested in applying for the Specialist I – Clinical Safety role should meet the following academic and professional requirements. Educational Qualification Bachelor’s, Master’s, or PharmD degree in relevant scientific disciplines. Relevant educational backgrounds include: BPharmacy, MPharmacy, PharmD, BSc Life Sciences, BSc Nursing, MSc Biotechnology, MSc Microbiology, MSc Biochemistry, MSc Pharmacology, MSc Clinical Research, MSc Life Sciences, Biological Sciences. Experience • 1–2 years of pharmacovigilance or drug safety experience including AE/SAE case processing OR • 2–5 years of experience in pharmaceutical, biotechnology, or CRO environments such as clinical data management, regulatory affairs, medical affairs, or quality assurance Technical Skills • Experience processing adverse event and serious adverse event reports • Knowledge of MedDRA coding and patient narrative writing • Understanding of pharmacovigilance safety databases • Familiarity with Good Clinical Practice (GCP) guidelines • Knowledge of ICH pharmacovigilance regulations and global safety reporting requirements • Experience supporting safety reports such as PSUR and DSUR Professional Skills • High attention to detail and data accuracy • Strong written and verbal communication abilities • Ability to work independently with minimal supervision • Good teamwork and collaboration skills • Strong organizational and documentation skills Professionals experienced in pharmacovigilance case processing, clinical trial safety documentation, regulatory safety reporting, and drug safety surveillance will find this role well aligned with long‑term careers in clinical research and global CRO organizations. Location and Salary Location: Bangalore, Karnataka, India Work Environment: Office‑based clinical safety operations role Salary: Competitive salary package based on experience and CRO industry standards. Employees working with Fortrea gain exposure to global drug safety operations, regulatory pharmacovigilance frameworks, and international clinical research programs. Application Process Candidates interested in applying for the Specialist I – Clinical Safety role can submit their application through the official Fortrea careers portal. Apply Here: https://careers.fortrea.com/us/en/job/26731/Specialist-I Applicants are encouraged to apply early as pharmacovigilance roles within global CRO organizations typically receive a high number of qualified applications. Frequently Asked Questions What does a Clinical Safety Specialist do? A Clinical Safety Specialist manages adverse event reports, performs pharmacovigilance case processing, writes patient narratives, and ensures regulatory safety reporting compliance during clinical trials and post‑marketing drug monitoring. Who can apply for the Fortrea Specialist I role? Candidates with degrees in pharmacy, life sciences, biotechnology, nursing, or medical sciences with pharmacovigilance or clinical research experience can apply. What is AE and SAE processing in pharmacovigilance? AE and SAE processing involves reviewing safety reports, entering case data into pharmacovigilance systems, coding medical terms using MedDRA, and reporting safety events to regulatory authorities. What regulatory guidelines are important for this role? Knowledge of Good Clinical Practice (GCP), ICH pharmacovigilance guidelines, and global regulatory reporting requirements is important for performing drug safety operations. Where is the job located? The role is located in Bangalore, India, within Fortrea’s clinical safety and pharmacovigilance operations team. Job Summary Category Details Company Fortrea Vacancies Specialist I – Clinical Safety Required Education BPharmacy, MPharmacy, PharmD, BSc Life Sciences, BSc Nursing, MSc Biotechnology, MSc Microbiology, MSc Biochemistry, MSc Pharmacology, MSc Clinical Research, MSc Life Sciences Experience 1–2 years Pharmacovigilance or 2–5 years Pharmaceutical/CRO experience [...] Read more...

Fortrea Hiring Fresher Pharmacovigilance – Safety Science Analyst

March 13, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Fortrea Hiring Safety Science Analyst – Pharmacovigilance Fresher Opportunity in Pune Fortrea is currently hiring for the position of Safety Science Analyst in Pune, India. This is a 6‑month contract role within the Clinical Safety / Pharmacovigilance department, designed primarily for healthcare and life sciences graduates who want to begin their careers in drug safety and pharmacovigilance operations. The opportunity is open to candidates with 0–1 year of safety experience, making it suitable for freshers and early‑career professionals interested in clinical safety, adverse event reporting, and global pharmacovigilance processes. The Safety Science Analyst will assist in handling safety data collected from clinical trials and post‑marketing surveillance programs, ensuring accurate processing of adverse events and compliance with regulatory reporting timelines. This role provides exposure to global safety databases, regulatory guidelines, and the end‑to‑end pharmacovigilance workflow used in modern pharmaceutical development. Professionals selected for this role will collaborate with global clinical safety teams, regulatory specialists, and pharmacovigilance experts to ensure patient safety information is processed accurately and efficiently. For candidates aiming to build careers in drug safety, clinical research, pharmacovigilance operations, and regulatory compliance, this role provides an excellent entry point into the pharmaceutical industry. Company Overview Fortrea is a global contract research organization (CRO) that supports pharmaceutical, biotechnology, and medical device companies throughout the clinical development lifecycle. The organization specializes in clinical trial management, pharmacovigilance, regulatory support, and data science services that help bring new medicines and therapies to patients faster. With decades of experience in clinical development, Fortrea partners with healthcare companies worldwide to manage clinical trials, monitor drug safety, and ensure compliance with international regulatory standards. The company operates across multiple therapeutic areas including oncology, cardiovascular diseases, neurology, immunology, and rare diseases. Fortrea’s pharmacovigilance and safety science teams play a critical role in monitoring adverse events, analyzing safety signals, and ensuring medicines meet global regulatory safety requirements. Through its global network of safety experts and clinical researchers, the organization contributes to improving patient outcomes and ensuring the safe use of medicines across international markets. Employees working at Fortrea gain exposure to advanced safety reporting systems, global clinical trial environments, and regulatory frameworks used by leading pharmaceutical companies worldwide. Job Role & Responsibilities The Safety Science Analyst supports pharmacovigilance and clinical safety operations by assisting with the collection, processing, and reporting of safety data related to pharmaceutical products. Key responsibilities include: Performing intake and triage of incoming safety reports from clinical trials and spontaneous reporting systems Processing adverse event reports according to regulatory guidelines and company procedures Entering safety data into adverse event tracking systems and pharmacovigilance databases Preparing patient narratives that summarize safety case information Coding adverse events using the MedDRA dictionary where applicable Supporting assessment of listedness against product labeling for marketed products Generating queries to obtain missing or inconsistent safety information Coordinating with medical reviewers and pharmacovigilance staff to resolve case queries Submitting expedited serious adverse event (SAE) reports to clients, investigators, and regulatory authorities Supporting submission of periodic safety reports and regulatory documentation Assisting with reconciliation of clinical safety databases Maintaining documentation related to global adverse event reporting requirements Supporting archival and documentation management for safety case files Ensuring compliance with internal quality systems, including SOPs and work instructions Collaborating with cross‑functional teams within pharmacovigilance and clinical safety departments This role ensures that adverse event data is captured accurately and reported within regulatory timelines, helping protect patient safety and maintain compliance with global drug safety regulations. Eligibility / Qualifications Candidates applying for this pharmacovigilance and clinical safety role should meet the following requirements. Required Education Candidates must hold a healthcare or life sciences degree. Relevant courses include: B.Pharm, M.Pharm, PharmD, BAMS, BDS, BHMS, Nursing, Pharmacology, Clinical Research, Life Sciences Experience 0–1 year of experience in pharmacovigilance or drug safety operations Freshers with healthcare or pharmacy backgrounds are eligible to apply Required Skills Strong attention to detail when handling clinical safety data Good written and verbal communication skills Ability to manage multiple safety cases and deadlines Knowledge of pharmacovigilance processes and adverse event reporting Familiarity with Microsoft Office tools and data entry systems Ability to work collaboratively in clinical safety teams Preferred Knowledge Basic understanding of MedDRA coding and pharmacovigilance terminology Awareness of regulatory safety reporting guidelines Location & Salary Job Location: Pune, Maharashtra, India Work Model: Office based role This position is offered as a 6‑month contract opportunity within Fortrea’s clinical safety operations team. Salary details for this position have not been publicly disclosed. Compensation typically depends on company policy and the candidate’s educational background or prior safety experience. Application Process Candidates interested in this pharmacovigilance job opportunity can apply through the official Fortrea careers portal. Apply here: https://careers.fortrea.com/us/en/job/261157/Safety-Science-Analyst-6-months-contract-Bengaluru-HCP-only Applicants are advised to submit their applications through the official website to ensure authenticity and avoid recruitment scams. Frequently Asked Questions What does a Safety Science Analyst do? A Safety Science Analyst processes adverse event reports, enters safety data into pharmacovigilance systems, prepares patient narratives, and supports regulatory reporting for clinical trials and marketed medicines. Who can apply for this role? Candidates with healthcare or pharmacy degrees such as B.Pharm, M.Pharm, PharmD, BAMS, BDS, BHMS, or Nursing can apply. Is this role suitable for freshers? Yes. Candidates with 0–1 year of safety or pharmacovigilance experience can apply for this role. What systems are commonly used in pharmacovigilance roles? Pharmacovigilance professionals typically work with safety databases, adverse event reporting systems, and coding dictionaries such as MedDRA. How can I apply for this job? Candidates can apply through the official Fortrea careers website using the application link provided above. Job Summary Company Fortrea Vacancies Safety Science Analyst Required Education B.Pharm, M.Pharm, PharmD, BAMS, BDS, BHMS, Nursing, Pharmacology, Clinical Research, Life Sciences Experience 0–1 year pharmacovigilance or safety experience [...] Read more...

ICON Plc Pharmacovigilance Entry Level Vacancies: Pharmacovigilance Assistant I

March 13, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Are you looking to kick-start your career in pharmacovigilance? ICON Plc is offering entry-level vacancies for Pharmacovigilance Assistants in Chennai. Join our team at the Drug Safety ICON Full Service & Corporate Support Office and be a part of our mission to advance and improve patients’ lives. About ICON ICON is driven by a culture of accountability, collaboration, partnership, and integrity. We aim to be the Clinical Research Organisation that delivers excellence to our clients and patients at every touch-point. If you share our vision and are passionate about making a difference in healthcare, we invite you to join us. Pharmacovigilance Assistant I Job Responsibilities As a Pharmacovigilance Assistant at ICON Plc, your responsibilities will include: Business Support: Receives and distributes incoming safety notifications (such as exception approvals, hospital records, SAEs, SAE Hotline calls and other safety events via eFax, e-mail and safety mailboxes) to the appropriate project teams or to Sponsor contacts as per assignment; or surveillance of Safety Reporting specific mailboxes. Initiates appropriate actions to protect data privacy with regards to received unrequested personal identifiers. Maintains data entry for SAEs and miscellaneous tracking logs for all current projects. Prepares and submits courier shipments and electronic safety submissions on behalf of the project teams, including acknowledgement uploads to Safety Reporting System and maintenance of address data for safety submissions. Case tracker management and support Distribution of safety related documents like Clinical Trial Application (CTA), Power of Attorney (PoA) or delegation documents, and website searches as support to the safety reporting intelligence team. Uploads documents into the electronic Trial Master File (eTMF) and tracks the status in the Safety Tracking Tools. Downloads Safety Reporting Post-Marketing ICSR. Completes EudraVigilance acknowledgement of receipt (AoR) tracking in Safety Reporting System. Safety Reporting (CA Country Portal submissions, Monitoring of mailboxes and/or Client Portal, Support for expedited and periodic reporting and Bulk report submission and reconciliation) Performs the Translation Management Process as assigned. Perform regular testing of SAE Hotline, departmental phone lines, fax numbers and email addresses (general and project specific) as required; documents results. Maintain departmental and global calendars as required. Completion of monthly metrics. Perform offsite archiving activities as required. Applies knowledge and adheres to company policies and procedures including corporate guidelines and best practices. Flag errors/non-conformance to established processes. Applies knowledge of computerized information systems and standard application software (Windows, MS Office). Identifies and recognizes problems that have established precedents and limited impact. Refers non-standard questions and problems to higher levels. Project Management Support: Organizes project team and client meetings including scheduling, agendas, preparation of presentations and meeting minutes. Organizes, reviews and manages project specific information and material following applicable company processes, (such as organizational charts, Project Management Plans, project status reports). Supports the Project Manager with financial tasks. Support and processes purchase orders and project invoices. Acts as gatekeepers for eTMF and project file and maintains project specific email distribution lists. Uploads and files all documents within allotted timeframe into the electronic Trial Master File (eTMF) or Trial Master File (TMF), including package preparation, reconciliation of the TMF and the safety tracking tools for inspection readiness, sampling and coherence QC and query resolution and follow up. Monitoring and filing of project specific mailboxes. Maintains a training matrix, including assigning and tracking project-specific training and tracking training compliance as applicable in the relevant system(s). Maintenance, coordination and access of project Enterprise Document and Content Management Systems (EDCMS) and mapped drives etc. Monitors project team’s approved Curriculum Vitae (CV) dates in eTMF or Project File for compliance with applicable SOP. Updates project metrics and team members in applicable systems. Perform other activities as identified and requested by management. Benefits of Working at ICON We offer competitive salary packages, annual bonuses, health-related benefits, retirement plans, and a supportive environment that encourages talent and high performance. ICON is an equal opportunity and inclusive employer committed to providing a workplace free of discrimination and harassment. Join us at ICON Plc in Chennai and embark on a rewarding career journey in pharmacovigilance. Apply now to be part of our dynamic team and contribute to shaping the future of drug safety. Apply Online [...] Read more...

Novartis hiring Info Specialist – Literature Intelligence

March 11, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Novartis hiring Info Specialist – Literature Intelligence in Hyderabad. Pharmacy, Life Sciences graduates with 3–5 years experience eligible. Novartis is hiring an Info Specialist – Literature Intelligence for its Development division in Hyderabad, India. This role is ideal for experienced pharmacy and life sciences professionals who specialize in scientific literature search, medical intelligence, and pharmaceutical information management. The position plays a critical role in supporting pharmacovigilance, medical affairs, drug development, and regulatory decision-making through high-quality literature intelligence and advanced bibliographic analysis. Company Overview Novartis is one of the world’s leading pharmaceutical companies, known for its strong focus on innovation, patient-centric research, and ethical scientific practices. With a global presence across drug development, regulatory science, and healthcare innovation, Novartis consistently ranks among the most trusted and valued medicines companies worldwide. In India, Novartis Healthcare Private Limited supports global operations through advanced research, development, and knowledge services. The organization invests heavily in data-driven decision-making, medical intelligence, and scientific excellence, making it a preferred employer for experienced pharma and life sciences professionals. Job Role & Responsibilities As an Info Specialist – Literature Intelligence, you will provide expert-level literature search and analysis support across pharmacovigilance, medical affairs, medical information, and drug development teams. Your work directly contributes to regulatory submissions, health authority responses, formulary reviews, and evidence-based medical decision-making. Key Responsibilities Conduct advanced pharmaceutical and biomedical literature searches using global databases Develop precise and reproducible search strategies covering drug nomenclature, drug classes, and competitive intelligence Curate and analyze scientific and technical literature to support regulatory submissions and health agency requests Deliver timely, high-quality literature intelligence insights to cross-functional global teams Perform comprehensive literature reviews for product submissions, safety assessments, and formulary evaluations Maintain expertise in advanced bibliographic and information management practices Manage citations and references using tools such as EndNote and Mendeley Create and maintain alert strategies for ongoing scientific surveillance Collaborate with global stakeholders to ensure consistency and quality in literature intelligence delivery This role requires deep expertise in pharmaceutical information sciences and supports critical decision-making in drug safety, development, and commercialization. Eligibility / Qualifications Required Education Candidates must hold an advanced scientific qualification in one of the following: Pharmacy, Life Sciences, Pharmacology, Biology, Biotechnology, Biomedical Sciences Essential Experience 3 to 5 years of relevant experience in pharmaceutical industry, research organizations, or corporate information centers Proven expertise in scientific literature searching and information analysis Hands-on experience with pharmaceutical and biomedical databases such as OVID, Embase, Medline, PubMed, Cortellis, and PharmaProjects Strong understanding of medical terminology and pharmaceutical research workflows Experience supporting pharmacovigilance, medical affairs, or regulatory teams Preferred Skills Knowledge of text mining, natural language processing (NLP), and knowledge graphs Strong written and verbal communication skills Ability to prepare clear literature summaries and presentations for scientific audiences Experience working with global, cross-functional teams Location & Salary Location: Hyderabad, Telangana, India Work Model: Hybrid (#LI-Hybrid) Employment Type: Full-time, regular Shift Work: No Application Process Interested and eligible candidates should apply through the official Novartis careers portal: Apply Online: https://www.novartis.com/careers/career-search/job/details/req-10063537-info-specialist-literature-intelligence Ensure your resume highlights pharmaceutical database expertise, literature search methodologies, and experience supporting regulatory or medical teams. Frequently Asked Questions (FAQs) Is this role suitable for freshers? No. This position requires 3–5 years of relevant pharmaceutical or research experience. What databases should candidates be familiar with? Candidates should have experience with databases such as PubMed, Embase, OVID, Medline, Cortellis, and PharmaProjects. Is this a pharmacovigilance role? This is not a direct pharmacovigilance role, but it strongly supports pharmacovigilance and regulatory safety activities. Is the role remote? This is a hybrid role based in Hyderabad, combining office-based and digital work. What is the career progression after this role? Career growth includes Senior Information Specialist, Literature Intelligence Lead, Medical Information Manager, and Regulatory Knowledge roles. Equal Employment Opportunity Novartis is committed to building an inclusive, diverse, and non-discriminatory workplace aligned with global employment standards. Job Summary Table Company Novartis Healthcare Private Limited Vacancies Info Specialist – Literature Intelligence Required Education Pharmacy, Life Sciences, Pharmacology, Biology, Biotechnology, Biomedical Sciences Experience 3–5 Years [...] Read more...

Alvotech Hiring Pharmacovigilance Associate – (Partially Remote Job)

March 11, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Alvotech Hiring Pharmacovigilance Associate – Drug Safety Jobs in Bangalore (Partially Remote) Alvotech is inviting applications for the position of Pharmacovigilance Associate – Safety Data Management within its Global Safety and Clinical Research division. This opportunity is based in Bangalore with a partially remote work model and is ideal for professionals with experience in pharmacovigilance, drug safety monitoring, and clinical safety data management. The vacancy is part of the Integrated Clinical and Medical Research (iCMR) department, which focuses on developing effective clinical strategies for biosimilar medicines and ensuring compliance with international regulatory standards. Candidates with 2+ years of experience in pharmacovigilance or clinical safety management and a postgraduate qualification in pharmaceutical sciences or life sciences are encouraged to apply. This role offers an excellent opportunity to work in the rapidly growing biopharmaceutical and biosimilars industry, contributing to global drug safety monitoring and regulatory compliance activities that directly support patient safety worldwide. Company Overview Alvotech is a fully integrated biopharmaceutical company specializing in biosimilar development and manufacturing. The company focuses on delivering high‑quality biosimilar medicines that expand patient access to life‑saving treatments while reducing healthcare costs globally. Headquartered internationally and operating across multiple global markets, Alvotech collaborates with pharmaceutical partners and regulatory agencies to bring safe and effective biosimilar therapies to patients. Within the organization, the Integrated Clinical and Medical Research (iCMR) department leads the planning and execution of clinical trials, regulatory compliance strategies, and post‑marketing safety programs. The department aligns clinical development with global biosimilar guidelines and regulatory requirements issued by authorities such as the FDA, EMA, and international regulatory bodies. By joining Alvotech, professionals gain the opportunity to work with advanced pharmacovigilance technologies, safety databases, and global clinical research programs supporting biologics and biosimilar therapies. Job Role and Responsibilities The Pharmacovigilance Associate – Safety Data Management will support clinical safety monitoring activities for both clinical trials and post‑marketing pharmacovigilance programs. The role focuses on maintaining accurate safety data, ensuring regulatory compliance, and supporting global drug safety operations. The position operates within the Global Safety Data Management team and reports to the Safety Data Management Director. Core Responsibilities • Manage assigned pharmacovigilance tasks related to clinical trial safety and post‑marketing drug safety monitoring • Handle Individual Case Safety Reports (ICSR) and Serious Adverse Event (SAE) management activities • Support regulatory safety submissions to global health authorities • Perform literature monitoring and digital safety surveillance for drug safety signals • Conduct reconciliation activities between clinical safety databases and external partners • Manage EudraVigilance (EV) and XEVMPD related activities where applicable • Participate in the configuration, validation, and lifecycle management of pharmacovigilance systems • Maintain and optimize global pharmacovigilance processes aligned with international regulations • Ensure compliance with global pharmacovigilance standards including FDA, EMA, and ICH guidelines • Collaborate with cross‑functional teams including clinical trials, regulatory affairs, quality assurance, and benefit‑risk management • Coordinate with pharmacovigilance service providers and global business partners • Deliver training programs related to pharmacovigilance processes and safety compliance standards • Support internal and external audits and regulatory inspections related to safety data management Through these responsibilities, the Pharmacovigilance Associate contributes to maintaining patient safety by ensuring accurate monitoring, reporting, and evaluation of drug safety information. Eligibility and Qualifications Candidates interested in the Pharmacovigilance Associate role should meet the following educational and professional criteria. Educational Qualification Master’s Degree in pharmaceutical sciences or related healthcare disciplines. Relevant educational backgrounds include: MPharmacy, MSc Pharmacology, MSc Clinical Research, MSc Biotechnology, MSc Microbiology, MSc Biochemistry, MSc Life Sciences, PharmD, MSc Pharmaceutical Sciences, MSc Biomedical Sciences. Experience • Minimum 2 years of experience in pharmacovigilance or drug safety operations • Hands‑on experience in clinical trial safety monitoring and post‑marketing pharmacovigilance activities Technical Skills • Experience working with pharmacovigilance safety databases such as Argus Safety, ARISg, or Veeva Safety Vault • Knowledge of pharmacovigilance regulations including 21 CFR, ICH guidelines, GVP, GCP, and CIOMS standards • Experience working with global pharmaceutical products and clinical trials • Understanding of safety data management lifecycle and regulatory reporting requirements • Familiarity with biologic or combination product safety monitoring is considered an advantage Professional Skills • Strong organizational and time‑management abilities • Excellent written and verbal communication skills • Ability to work independently and collaborate within multicultural teams • Strong analytical skills for evaluating clinical safety data • Ability to manage multiple pharmacovigilance tasks simultaneously in a dynamic environment • Willingness to travel internationally when required Professionals with experience in pharmacovigilance case processing, clinical safety data management, drug safety surveillance, and regulatory safety reporting will find this role highly aligned with long‑term careers in pharmaceutical safety science. Location and Salary Location: Bangalore, India Work Model: Partially Remote / Hybrid Application Process Candidates interested in applying for the Pharmacovigilance Associate – Safety Data Management role can submit their application through the official Alvotech careers portal. Apply Here: https://alvotech.wd103.myworkdayjobs.com/Alvotech_Careers/job/Bangalore-Office/Pharmacovigilance-Associate–Safety-Data-Management_JR100089 Applicants should apply before March 23, 2026 to be considered for this position. Frequently Asked Questions What does a Pharmacovigilance Associate do? A Pharmacovigilance Associate monitors drug safety information, processes adverse event reports, ensures regulatory compliance, and supports clinical trial and post‑marketing safety surveillance activities. Who can apply for this pharmacovigilance job? Candidates with a master’s degree in pharmacy, pharmacology, biotechnology, clinical research, or life sciences with at least two years of experience in drug safety or pharmacovigilance can apply. What safety systems are commonly used in pharmacovigilance? Common pharmacovigilance systems include Argus Safety, ARISg, and Veeva Safety Vault which help manage safety reports, regulatory submissions, and drug safety monitoring. Is this job suitable for freshers? No. This role requires at least two years of experience in pharmacovigilance or clinical safety operations. Where is the job located? The role is based in Bangalore, India, with a partially remote work model. Job Summary Category Details Company Alvotech Vacancies Pharmacovigilance Associate – Safety Data Management Required Education MPharmacy, MSc Pharmacology, MSc Clinical Research, MSc Biotechnology, MSc Microbiology, MSc Biochemistry, MSc Life Sciences, PharmD, MSc Pharmaceutical Sciences, MSc Biomedical Sciences Experience Minimum 2+ years in Pharmacovigilance or Drug Safety [...] Read more...

Pharmacovigilance Drug Safety Associate in Hyderabad – Azurity Pharmaceuticals

March 10, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Azurity Pharmaceuticals Hiring Drug Safety Associate in Hyderabad – Life Science Graduates Apply Azurity Pharmaceuticals has announced a new hiring opportunity for the position of Associate, Drug Safety – Quality, Standards & Training in the Global Drug Safety department. The vacancy is based in Hyderabad and is open to life science graduates with relevant pharmacovigilance or drug safety experience. This role offers a strong career pathway for candidates looking to build expertise in pharmacovigilance, regulatory compliance, and drug safety quality systems within a global pharmaceutical organization. The recruitment drive highlights the growing demand for professionals in pharmacovigilance and drug safety operations, especially as pharmaceutical companies strengthen patient safety monitoring and regulatory compliance frameworks worldwide. Company Overview Azurity Pharmaceuticals is a specialty pharmaceutical company focused on developing innovative and accessible medicines for patients with unmet medical needs. The company operates globally and has built a strong reputation for delivering high-quality formulations across multiple therapeutic segments. Its product portfolio includes treatments across cardiovascular, neurology, endocrinology, gastroenterology, institutional care, and orphan disease segments. With a strong commitment to scientific excellence and patient-centered innovation, Azurity continues to expand its late-stage development pipeline and commercial product portfolio. The company collaborates with global partners and regulatory bodies to ensure the highest standards of drug safety, pharmacovigilance compliance, and quality assurance across all stages of the product lifecycle. Career Outlook for Drug Safety Analysts in 2026 Drug safety and pharmacovigilance have become critical functions within the pharmaceutical and biotechnology industry. With increasing regulatory scrutiny from global health authorities, companies are investing heavily in pharmacovigilance infrastructure and compliance systems. In 2026, the demand for drug safety professionals is expected to grow significantly as pharmaceutical companies expand clinical trials, global drug approvals, and post-marketing safety monitoring programs. Professionals trained in pharmacovigilance, safety database management, regulatory reporting, and quality systems are becoming essential for maintaining patient safety standards worldwide. Entry-level roles such as Drug Safety Associate or Safety Science Analyst often serve as the gateway to long-term careers in pharmacovigilance, regulatory affairs, and clinical safety leadership. Job Role & Responsibilities The Associate, Drug Safety – Quality, Standards & Training will support the Global Drug Safety organization in maintaining quality systems, training programs, and regulatory compliance standards. Key responsibilities include: Supporting the maintenance and administration of Drug Safety Standard Operating Procedures (SOPs), work instructions, and documentation standards Assisting with document updates, version control, and SOP lifecycle management Coordinating drug safety training programs including onboarding and refresher sessions Tracking training completion and maintaining training compliance records Supporting preparation for pharmacovigilance inspections and regulatory audits Assisting in maintaining inspection-ready documentation and training records Collaborating with Drug Safety Operations, Compliance, Quality Assurance, Regulatory Affairs, and Clinical teams Supporting communication of quality standards and training updates across drug safety teams Contributing to global initiatives related to standardized pharmacovigilance processes and training systems This role plays a key part in ensuring regulatory readiness and operational consistency within the global pharmacovigilance framework. Eligibility / Qualifications Candidates applying for this role should meet the following criteria: Required Experience 1–3 years of experience in pharmacovigilance, drug safety, quality compliance, training coordination, or related pharmaceutical roles Experience working with quality systems, SOP documentation, or training administration is preferred Understanding of pharmacovigilance processes and regulated pharmaceutical environments Educational Qualification Bachelor’s degree in Life Sciences or related fields. Relevant courses include: B.Pharm, M.Pharm, Pharm.D, BSc Life Sciences, BSc Biotechnology, BSc Microbiology, BSc Biochemistry, MSc Biotechnology, MSc Microbiology, MSc Biochemistry, MSc Clinical Research, MSc Life Sciences. Candidates with knowledge of drug safety databases, regulatory guidelines, and pharmacovigilance quality systems will have an advantage. Location & Salary Location: Hyderabad, India Salary: Competitive salary package based on experience and industry standards. Candidates may also receive additional benefits depending on company policies. Hyderabad continues to be a major hub for pharmaceutical companies, pharmacovigilance centers, and global capability centers, offering strong long-term career opportunities in drug safety and regulatory science. Application Process Interested candidates can apply online through the official application portal using the link below: Apply Here: https://job-boards.greenhouse.io/azuritypharmaceuticalsindia/jobs/4669785005?gh_src=kVJ1uA Applicants are encouraged to apply early as pharmaceutical companies often review applications on a rolling basis. Frequently Asked Questions (FAQs) Who can apply for the Drug Safety Associate role at Azurity Pharmaceuticals? Candidates with a Bachelor’s degree in Life Sciences such as B.Pharm, M.Pharm, Pharm.D, BSc Biotechnology, Microbiology, Biochemistry, or related fields with 1–3 years of pharmacovigilance or quality experience can apply. Is pharmacovigilance experience mandatory? Candidates with pharmacovigilance, drug safety, quality systems, compliance, or training coordination experience in pharmaceutical or biotech companies are preferred. What skills are important for this role? Key skills include knowledge of pharmacovigilance processes, SOP documentation, regulatory compliance, training coordination, audit preparation, and cross-functional collaboration. Where is the job located? The position is based in Hyderabad, one of India’s leading pharmaceutical and life sciences industry hubs. How do I apply for this role? Candidates can submit their application online through the official Azurity Pharmaceuticals recruitment portal using the provided link. Summary Company Azurity Pharmaceuticals Vacancies Associate – Drug Safety (Quality, Standards & Training) Required Education B.Pharm, M.Pharm, Pharm.D, BSc Life Sciences, Biotechnology, Microbiology, Biochemistry, MSc Biotechnology, MSc Microbiology, MSc Biochemistry, MSc Clinical Research Experience 1–3 Years Pharmacovigilance / Drug Safety / Quality Compliance [...] Read more...

Associate Pharmacovigilance Specialist Vacancies at Clarivate, Noida

March 9, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Clarivate Hiring Associate Pharmacovigilance Specialist for Pharma Graduates Global life science analytics company Clarivate has opened hiring for the role of Associate Pharmacovigilance Specialist in Noida, creating an exciting opportunity for pharmacy and life science graduates interested in drug safety and pharmacovigilance careers. For B.Pharm, M.Pharm and biomedical science graduates, this role provides early exposure to pharmacovigilance operations, biomedical literature monitoring, and adverse event identification. These roles play a critical role in protecting patient safety by identifying potential drug risks reported in scientific literature and clinical studies. As pharmaceutical companies continue to strengthen global drug safety monitoring, pharmacovigilance professionals are becoming essential to regulatory compliance and risk management across the healthcare industry. Company Overview Clarivate is a global information services and analytics company providing trusted data, insights, and solutions to accelerate innovation across the life sciences and healthcare industries. The company supports pharmaceutical organizations with drug safety monitoring, scientific data analysis, and regulatory intelligence. Clarivate works with global pharmaceutical companies, research organizations, and healthcare innovators to help improve drug development efficiency, regulatory compliance, and patient safety outcomes. The pharmacovigilance team at Clarivate supports multiple global clients across various therapeutic areas and focuses on identifying safety signals, monitoring biomedical literature, and supporting regulatory safety reporting activities. Career Outlook for Safety Science Analysts in 2026 The demand for pharmacovigilance and drug safety professionals is expected to increase significantly by 2026 as pharmaceutical companies face stricter global safety regulations. Regulatory authorities now require continuous monitoring of adverse events reported in clinical trials, post‑marketing data, and published biomedical literature. Safety science analysts and pharmacovigilance specialists are responsible for detecting safety signals, evaluating adverse drug reactions, and supporting risk management strategies for pharmaceutical products. Professionals who start their careers in pharmacovigilance often progress into roles such as Drug Safety Associate, Pharmacovigilance Scientist, Safety Data Analyst, Medical Safety Reviewer, or Global Drug Safety Manager. With the growth of global clinical trials and increasing volumes of medical literature, professionals skilled in biomedical literature review, safety database management, and adverse event reporting will remain highly valuable across the pharmaceutical industry. Job Role & Responsibilities The Associate Pharmacovigilance Specialist will support drug safety monitoring through biomedical literature review and identification of adverse event reports. Key responsibilities include: Review biomedical literature to identify potential adverse event reports related to pharmaceutical products Analyze scientific publications to detect Individual Case Safety Reports (ICSRs) Write concise narratives summarizing safety information from published literature Assess safety‑relevant information that could impact drug risk‑benefit profiles Track and document pharmacovigilance activities using drug safety systems Ensure compliance with pharmacovigilance regulations and internal SOPs Complete literature review batches accurately within defined timelines These activities help ensure that pharmaceutical companies remain compliant with international drug safety monitoring requirements. Eligibility / Qualifications Candidates applying for this pharmacovigilance opportunity should meet the following requirements: Master’s degree in Life Sciences, Pharmacy, Biomedical Sciences, Biotechnology, Microbiology, Biochemistry, or related fields Strong understanding of biomedical terminology and therapeutic areas Ability to analyze scientific articles and extract safety information Strong written communication skills for safety narrative writing Relevant education backgrounds include: M.Pharm, PharmD, M.Sc Biotechnology, M.Sc Microbiology, M.Sc Biochemistry, M.Sc Biomedical Sciences, B.Pharm with pharmacovigilance knowledge. Experience Clarivate is open to early‑career professionals. Freshers or candidates with up to 2 years of pharmacovigilance or biomedical literature review experience Experience working with biomedical databases or drug safety systems is an advantage Knowledge of adverse event reporting processes is beneficial Candidates with strong scientific reading ability and interest in drug safety are encouraged to apply. Skills & Competencies Candidates should demonstrate the following capabilities: Strong analytical ability to review and summarize scientific literature Understanding of biomedical terminology and pharmaceutical products Effective time management and ability to handle large volumes of literature Excellent written and verbal communication skills Ability to work in fast‑paced pharmacovigilance environments Location & Work Model Location: Noida, Uttar Pradesh, India Work Mode: Hybrid work model Working Hours: Typically between 9:00 AM to 6:00 PM IST or 11:00 AM to 8:00 PM IST depending on team requirements. Application Process Interested candidates can apply through the official Clarivate careers portal using the link below. Apply here: https://careers.clarivate.com/job/CLACLAGBJREQ134096EXTERNALENGB/Associate-Pharmacovigilance-Specialist Applicants should submit an updated resume highlighting their knowledge of biomedical literature review, pharmacovigilance concepts, and scientific research analysis. Early application is recommended as pharmacovigilance roles often attract large numbers of applicants from life science graduates. Frequently Asked Questions Who can apply for the Clarivate Associate Pharmacovigilance Specialist role? Candidates with master’s degrees in pharmacy, life sciences, biotechnology, microbiology, or biomedical sciences can apply. Is this role suitable for freshers? Yes. Freshers or candidates with up to two years of experience in pharmacovigilance or biomedical literature review are eligible. What does a pharmacovigilance specialist do? Pharmacovigilance specialists review safety data, monitor adverse event reports, and help pharmaceutical companies maintain regulatory compliance for drug safety. What career growth opportunities exist in pharmacovigilance? Professionals can progress into roles such as Drug Safety Associate, Pharmacovigilance Scientist, Medical Safety Reviewer, or Global Safety Manager. Summary Category Details Company Clarivate Vacancies Associate Pharmacovigilance Specialist Required Education M.Pharm, PharmD, M.Sc Biotechnology, M.Sc Microbiology, M.Sc Biochemistry Experience Freshers or up to 2 years in pharmacovigilance or literature review Location Noida, Uttar Pradesh Department Pharmacovigilance / Drug Safety [...] Read more...

Medical Coding Specialist Hiring Icon Plc | MedDRA, WhoDD

March 9, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now ICON Hiring Medical Coding Specialist for Clinical Data Management Teams Global clinical research organization ICON plc has announced hiring for the role of Medical Coding Specialist I across multiple Indian locations including Bengaluru, Chennai, and Trivandrum. The opportunity is designed for life science and healthcare graduates interested in clinical trial data management and medical coding within global drug development programs. For pharmacy and life science graduates looking to enter the clinical research industry, medical coding roles provide a strong entry into clinical data management and regulatory compliant data processing. Professionals working in this field help ensure that medical terms, adverse events, and drug information collected during clinical trials are accurately classified according to international coding standards. With pharmaceutical companies increasingly relying on accurate clinical trial data for regulatory submissions, medical coding specialists play an essential role in maintaining the integrity and reliability of global clinical research databases. Company Overview ICON plc is a world-leading healthcare intelligence and clinical research organization that supports pharmaceutical, biotechnology, and medical device companies throughout the drug development lifecycle. The company offers services in clinical development, clinical data management, pharmacovigilance, regulatory strategy, and real-world evidence generation. Operating across multiple countries, ICON collaborates with global pharmaceutical sponsors to accelerate clinical trials and support the approval of innovative medicines. The organization combines scientific expertise with advanced clinical technologies to manage complex clinical research programs. ICON’s clinical data management and medical coding teams ensure that data generated during clinical trials is standardized, accurate, and compliant with regulatory guidelines required by health authorities such as the US FDA, EMA, and other global agencies. Career Outlook for Safety Science Analysts and Medical Coding Professionals in 2026 The global clinical research industry continues to expand as pharmaceutical companies invest heavily in new therapies, vaccines, and precision medicines. By 2026, experts predict a growing demand for professionals specializing in clinical data management, safety science analytics, and medical coding. Medical coding specialists play a critical role in organizing clinical trial data by translating medical terms, diagnoses, and adverse events into standardized coding dictionaries such as MedDRA and WHO Drug. These coded datasets allow statisticians, safety scientists, and regulatory teams to analyze clinical trial outcomes efficiently. Professionals who begin careers in medical coding often progress into roles such as Clinical Data Manager, Drug Safety Associate, Pharmacovigilance Specialist, or Clinical Data Scientist. As clinical trials generate larger datasets, the need for skilled professionals capable of managing medical terminology and regulatory coding standards will continue to grow. Job Role & Responsibilities The Medical Coding Specialist will support clinical trial data quality by accurately coding medical terms and ensuring consistency across study datasets. Key responsibilities include: Code medical terms, diagnoses, and procedures using standardized coding dictionaries such as MedDRA and WHO Drug Ensure consistent medical coding across multiple clinical trials and research programs Review clinical data entries to identify and resolve coding discrepancies Collaborate with clinical data managers, statisticians, and safety teams to maintain accurate datasets Provide guidance on coding standards and conventions used during clinical research Maintain updated knowledge of medical coding guidelines and regulatory requirements Contribute to process improvements that enhance the quality and efficiency of clinical trial data coding These responsibilities help ensure that clinical trial datasets remain reliable and suitable for statistical analysis, regulatory submissions, and drug safety monitoring. Eligibility / Qualifications Candidates interested in this clinical research career opportunity should meet the following qualifications: Bachelor’s degree in Life Sciences, Pharmacy, Healthcare, or related discipline Understanding of medical coding systems such as MedDRA and WHO Drug Knowledge of clinical trial processes and clinical data management workflows Strong analytical thinking and attention to detail Good communication skills and ability to collaborate with cross-functional teams Relevant education backgrounds may include: B.Pharm, M.Pharm, B.Sc Biotechnology, B.Sc Microbiology, B.Sc Biochemistry, B.Sc Life Sciences, M.Sc Clinical Research, M.Sc Biotechnology, PharmD. Location & Salary Location: Bengaluru, Chennai, and Trivandrum, India Work Model: Office or hybrid work environment depending on project requirements. Salary: Competitive clinical research industry salary based on experience and technical expertise. Leading CRO companies typically provide structured compensation packages, healthcare benefits, and professional development opportunities. Benefits ICON offers a range of employee benefits designed to support professional growth and work-life balance. Benefits may include: Competitive salary and performance incentives Health insurance coverage for employees and families Retirement planning programs Global employee assistance support services Paid leave and flexible work arrangements Professional training and career development opportunities These benefits support employees working in high-impact clinical research environments across global projects. Application Process Interested candidates can apply through the official ICON careers portal using the link below. Apply here: https://careers.iconplc.com/job/medical-coding-specialist-in-india-bangalore-jid-48901 Applicants should submit an updated resume highlighting their knowledge of clinical research, medical terminology, and medical coding systems. Early applications are recommended as clinical data management roles in global CRO organizations often receive strong interest from qualified candidates. Frequently Asked Questions Who can apply for the ICON Medical Coding Specialist role? Candidates with degrees in pharmacy, life sciences, healthcare, or related fields with knowledge of medical terminology and coding systems can apply. Which coding dictionaries are used in clinical trials? Clinical trials commonly use standardized medical dictionaries such as MedDRA and WHO Drug for coding medical terms and adverse events. Is medical coding important for clinical research? Yes. Accurate medical coding ensures that clinical trial data is standardized and suitable for statistical analysis, safety monitoring, and regulatory submissions. What career growth opportunities exist in medical coding? Professionals can advance into roles such as Clinical Data Manager, Pharmacovigilance Specialist, Drug Safety Associate, or Clinical Data Scientist. Summary Category Details Company ICON plc Vacancies Medical Coding Specialist I Required Education B.Pharm, M.Pharm, B.Sc Biotechnology, B.Sc Microbiology, B.Sc Biochemistry, PharmD Experience Knowledge or experience in medical coding and clinical research Location Bengaluru, Chennai, Trivandrum Department Clinical Data Management [...] Read more...

Fresher Pharmacovigilance Vacancies at IQVIA

February 6, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now IQVIA, a leading global provider of advanced analytics, technology solutions, and clinical research services, is offering an exciting opportunity for fresh graduates to join our team as Safety Associate Trainees. Based in Bangalore offices, this role is ideal for individuals in the Kerala region who are eager to embark on a fulfilling career in drug safety and pharmacovigilance. IQVIA Safety Associate Trainee Opportunity Company Name: IQVIA Location: Kolkata, India Kochi, India Job Responsibilities: Job Overview Review, assess and process Safety data and information, across service lines, received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations SOPs and internal guidelines under guidance and support of senior operation team members. Location : Kolkata Job Type: Full-Time 𝑩𝒂𝒔𝒊𝒄 𝒓𝒆𝒒𝒖𝒊𝒓𝒆𝒎𝒆𝒏𝒕𝒔: ✅Recent graduates (freshers only) – 𝗠. 𝗣𝗵𝗮𝗿𝗺, 𝗕. 𝗣𝗵𝗮𝗿𝗺 & 𝗣𝗵𝗮𝗿𝗺 𝗗 𝗼𝗻𝗹𝘆. ✅Bangalore office based ✅Basic understanding of pharmacovigilance & clinical research. Job Responsibilities: As a drug Safety Associate Trainee at IQVIA, you will play a crucial role in ensuring the safety and well-being of patients by reviewing, assessing, and processing safety data and information. Your responsibilities will include: Prioritizing and completing assigned trainings on time to enhance your skills and knowledge. Processing safety data in compliance with applicable regulations, guidelines, and Standard Operating Procedures (SOPs). Performing Pharmacovigilance activities such as collecting and tracking incoming Adverse Events (AE)/endpoint information. Coding AE and products, writing narratives, and conducting literature-related activities. Collaborating with senior team members to ensure productivity and quality standards are met. Attending project team meetings and providing feedback to operations managers. Demonstrating 100% compliance towards all people practices and processes. Performing other duties as assigned to support project requirements. Qualifications: To qualify for this role, you must possess the following qualifications: High School Diploma or equivalent in a scientific or healthcare discipline. Bachelor’s Degree in a scientific or healthcare discipline preferred. Good knowledge of medical terminology and strong communication skills. Ability to work collaboratively in a team environment. Proficiency in Microsoft Office and web-based applications. Attention to detail and accuracy in work. Strong time management and multitasking abilities. Willingness to learn new skills and adapt to changing priorities. Flexibility to operate in shifts and occasional travel. About IQVIA: IQVIA is at the forefront of driving innovation and advancing human science in the life sciences industry. Our mission is to push the boundaries of data science to create impactful solutions that improve patient outcomes and healthcare delivery worldwide. By joining IQVIA, you’ll be part of a dynamic team dedicated to making a positive difference in people’s lives. Suppose you’re ready to take the next step in your career and contribute to meaningful projects that shape the future of healthcare. In that case, we encourage you to apply for the Safety Associate Trainee position at IQVIA. Join us in our mission to create a healthier world for all. Apply now! How to Apply: Apply LINK [...] Read more...

Merck hiring Pharmacovigilance Literature Surveillance & Reconciliation Analyst

January 13, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Literature Surveillance Analyst Vacancy Bangalore | PV Merck hiring Literature Surveillance & Reconciliation Analyst in Bangalore. Pharmacovigilance professionals with 3+ years experience. Merck is hiring a Literature Surveillance and Reconciliation Analyst for its R&D Excellence Center in Bangalore. This full-time role is ideal for experienced pharmacovigilance professionals who have worked in literature safety surveillance, ICSR reconciliation, and global patient safety operations. The position offers direct exposure to global drug safety systems, regulatory compliance, and cross-functional collaboration in an international research-driven environment. This opportunity is well suited for candidates looking to strengthen their long-term career in pharmacovigilance, patient safety, and regulatory compliance within a globally respected life science organization. Company Overview Merck is a global science and technology company operating across Healthcare, Life Science, and Electronics. With a strong heritage of innovation and responsibility, Merck focuses on advancing human progress through science-driven solutions that improve lives worldwide. The company’s Global Patient Safety teams play a critical role in ensuring the safe development and post-authorization monitoring of medicinal products. Merck operates under stringent global regulatory frameworks and maintains high standards of quality, compliance, and scientific integrity across its R&D and post-marketing activities. Working at Merck offers professionals exposure to international safety operations, robust regulatory systems, and a culture that values diversity, inclusion, and continuous learning. Job Role & Responsibilities The Literature Surveillance and Reconciliation Analyst will be part of the Global Patient Safety ICSR Management team and will support literature surveillance processes, reconciliation activities, and safety data quality management. Literature Surveillance Operations Support the business process owner for literature surveillance activities Perform operational tasks in the literature surveillance database, including reconciliation and quality control of non-ICSR literature Upload, manage, and track scientific articles in safety databases Conduct quality checks to ensure completeness, accuracy, and regulatory compliance of literature safety data ICSR Reconciliation and Safety Monitoring Perform ICSR reconciliation activities across relevant safety systems Conduct quality monitoring and spot checks of safety information in collaboration with cross-functional teams Ensure alignment between literature-derived safety data and ICSR records Support ongoing pharmacovigilance compliance and inspection readiness Systems, Training, and Access Management Support training documentation related to literature surveillance processes Manage user access and roles in literature surveillance and reconciliation databases Maintain system documentation in line with internal SOPs and regulatory expectations Communication and Coordination Manage and monitor team mailboxes to ensure timely action on incoming requests Coordinate with global stakeholders and functional teams to resolve safety-related queries Support smooth information flow within matrix teams operating across regions Eligibility / Qualifications Educational Qualification Candidates must hold a medical or scientific degree. Relevant courses include: MBBS, BPharm, MPharm, PharmD, MSc Life Sciences, MSc Pharmacology, MSc Clinical Research, PhD Life Sciences Experience Requirements Minimum 3 years of experience in a pharmacovigilance or patient safety environment Prior experience in literature safety surveillance and ICSR reconciliation is highly preferred Hands-on exposure to global drug safety regulations for development and post-authorization products Experience working with safety databases; exposure to ArisG safety database is an advantage Key Skills and Knowledge Strong understanding of global pharmacovigilance regulations and guidelines Knowledge of drug safety requirements for clinical and post-marketing products Excellent written and verbal communication skills Experience working in international and cross-cultural team environments Strong attention to detail and quality-focused mindset Location & Salary Job Location: Bangalore, Karnataka Employment Type: Full-time Work Model: Office-based / hybrid as per business requirements Salary: Competitive and aligned with industry standards for pharmacovigilance analyst roles Application Process Interested candidates can apply through the official Merck career portal using the link below: Apply here: https://careers.merckgroup.com/global/en/job/294925/Literature-Surveillance-and-Reconciliation-Analyst FAQs – Literature Surveillance and Reconciliation Analyst Who can apply for this role? Candidates with a medical or scientific degree and at least 3 years of pharmacovigilance experience can apply. Is this role suitable for freshers? No. Prior experience in literature surveillance or ICSR reconciliation is required. Does the role involve ICSR processing? The role focuses on reconciliation and quality monitoring rather than full end-to-end case processing. Is international exposure involved? Yes. The role involves collaboration with global teams in a matrix environment. What are the career growth opportunities? This role offers growth into senior patient safety, signal management, and global pharmacovigilance leadership positions. Summary Table Company Merck Vacancies Literature Surveillance and Reconciliation Analyst Required Education Medical / Scientific Degree (Pharmacy, Life Sciences, Medicine) Experience 3+ years in Pharmacovigilance / Patient Safety [...] Read more...

Vizen Life Sciences hiring Drug Safety Associate (ICSR)

January 13, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Drug Safety Associate Vacancy Pune | BPharm MPharm Vizen Life Sciences hiring Drug Safety Associate ICSR. BPharm/MPharm/PharmD with 1–3 years experience. Vizen Life Sciences Pvt Ltd is hiring a Drug Safety Associate (ICSR) for professionals looking to strengthen their career in pharmacovigilance and clinical safety operations. This full-time role is suitable for candidates with hands-on experience in individual case safety report processing, safety database activities, and regulatory-compliant drug safety workflows. The position offers exposure to global pharmacovigilance practices, client interactions, audits, and inspections, making it a strong opportunity for early- to mid-level drug safety professionals. Company Overview Vizen Life Sciences Pvt Ltd is a growing life sciences and pharmacovigilance services organization supporting pharmaceutical, biotechnology, and healthcare companies. The company focuses on delivering high-quality drug safety, regulatory compliance, and clinical support services aligned with global regulatory expectations. With a strong emphasis on quality, compliance, and client satisfaction, Vizen Life Sciences works closely with sponsors and CRO partners to ensure patient safety and data integrity across clinical and post-marketing activities. The organization provides structured learning, hands-on exposure, and long-term growth opportunities for professionals in pharmacovigilance and drug safety. Job Role & Responsibilities The Drug Safety Associate (ICSR) will be responsible for end-to-end processing of individual case safety reports and supporting pharmacovigilance activities in compliance with global regulatory standards. The role requires accuracy, attention to detail, and strong communication skills. ICSR Processing and Case Management Triage incoming safety reports for completeness, validity, and legibility Perform case booking and data entry of safety reports into the pharmacovigilance database Code adverse events, medical history, and medications using standard dictionaries Write clear, accurate, and compliant case narratives Request and manage follow-ups to obtain missing or additional safety information Literature and Safety Surveillance Perform literature searches to identify potential adverse event reports Review and document literature findings in line with pharmacovigilance requirements Support routine safety surveillance activities as assigned Client Interaction and Compliance Participate in client meetings and discussions related to drug safety activities Support preparation for audits and regulatory inspections Assist in follow-up activities after audits or inspections Ensure adherence to internal SOPs and global pharmacovigilance guidelines Skills and Competencies Strong analytical and problem-solving skills Ability to perform safety database searches and scientific literature reviews Excellent written and verbal communication skills Client-focused approach with attention to quality and timelines Ability to work in a regulated, process-driven environment Eligibility / Qualifications Educational Qualification Candidates must hold one of the following qualifications: BPharm, MPharm, or PharmD Relevant courses include: BPharm, MPharm (Pharmacology, Pharmaceutics), PharmD, MSc Pharmacology, MSc Clinical Research Experience Requirements 1 to 3 years of experience in Drug Safety or Pharmacovigilance Hands-on experience in ICSR processing and safety database activities Exposure to audits, inspections, or client interactions is an advantage Location & Salary Job Location: Not specified by employer Employment Type: Full-time Salary: As per industry standards and experience This role offers stable career growth in pharmacovigilance with exposure to global safety operations. Application Process Interested and eligible candidates can apply directly through the official company portal using the link below: Apply here: https://vizenlifesciences.keka.com/careers/jobdetails/43047?source=linkedin Early applications are encouraged as shortlisting may begin immediately. FAQs – Drug Safety Associate (ICSR) Who can apply for this Drug Safety Associate role? Candidates with BPharm, MPharm, or PharmD qualifications and 1–3 years of drug safety experience can apply. Is this role suitable for freshers? No. Prior experience in pharmacovigilance or ICSR processing is required. What type of work does ICSR involve? ICSR work includes case intake, data entry, coding, narrative writing, follow-ups, and literature review. Does the role involve audits and inspections? Yes. The role supports preparation for and participation in audits and regulatory inspections. What are the growth opportunities? This role provides a strong foundation for senior drug safety, signal management, and pharmacovigilance specialist positions. Summary Table Company Vizen Life Sciences Pvt Ltd Vacancies Drug Safety Associate (ICSR) Required Education BPharm, MPharm, PharmD Experience 1–3 years in Drug Safety / Pharmacovigilance [...] Read more...

Project Specialist Medical Affairs

January 28, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Project Specialist Medical Affairs Vacancy Hyderabad Bachelor’s degree Project Specialist Medical Affairs vacancy at Sanofi, Hyderabad. Apply for permanent pharma medical affairs role. Sanofi is hiring a Project Specialist – Medical Affairs for its Business Operations team in Hyderabad. This role is suited for life sciences and pharmaceutical professionals who want to work at the intersection of medical affairs, compliance, CRM systems, and global healthcare events management. The position offers exposure to global specialty care, vaccines, general medicines, and R&D functions while supporting scientifically driven engagements that directly impact patient outcomes worldwide. Working in a permanent, full-time capacity, the Project Specialist will support Sanofi’s medical and commercial organizations by managing compliant scientific events, advisory boards, and educational programs through structured project execution. This opportunity is ideal for candidates seeking long-term growth in pharmaceutical medical affairs operations within a globally respected biopharmaceutical company. Company Overview Sanofi is a leading global biopharmaceutical company focused on improving patient lives through innovative medicines, vaccines, and healthcare solutions. With a strong presence across immunology, diabetes, cardiovascular diseases, oncology, rare diseases, and transplant care, Sanofi delivers treatments relied upon by millions of patients across the world. Driven by science, digital innovation, and data-led decision-making, Sanofi continues to expand access to life-saving therapies while accelerating innovation through advanced technologies and AI-enabled platforms. The company operates with a strong commitment to ethics, compliance, diversity, and inclusion, making it a trusted name in global healthcare. Sanofi Business Operations (SBO), based in India, functions as a centralized strategic partner supporting global Medical Affairs, HEVA, Commercial, Specialty Care, Vaccines, General Medicines, Consumer Healthcare, and R&D teams. SBO plays a critical role in enabling compliant, efficient, and scalable medical and scientific engagements worldwide. Job Role & Responsibilities The Project Specialist – Medical Affairs plays a key operational role in planning, managing, documenting, and closing medical and scientific events in compliance with Sanofi’s global standards. The role requires strong project management, communication, and CRM system expertise, ensuring every engagement is executed efficiently while maintaining transparency and regulatory compliance. Key Responsibilities Medical Affairs Event Management Manage end-to-end medical and scientific events using a structured project approach Organize and document events within the 1CRM events portal Support advisory boards, consulting services, symposiums, speaker trainings, scientific education programs, hospital and clinical staff meetings, and third-party sponsorships CRM and Documentation Management Ensure all required documents and approvals are available prior to event creation Maintain accurate event data, attendee records, and documentation within the 1CRM system Manage event closure activities and post-event documentation Stakeholder Coordination Coordinate regularly with internal and external stakeholders until successful event execution Partner with event business requestors and engagement teams to ensure compliance Represent Sanofi consistently and professionally across all interactions Compliance and Governance Adhere strictly to company policies related to transparency, ethics, and regulatory compliance Ensure all medical affairs activities meet internal and external compliance standards Support audit readiness through accurate documentation and reporting Process Improvement and Reporting Provide recommendations for continuous process improvements Track KPIs and metrics to sustain operational synergies Support reporting requirements for leadership and global teams Training and Knowledge Management Mentor and train incoming rotating 1CRM digital asset specialists Develop, update, and maintain training guidelines and process documentation Stay updated on CRM system enhancements and participate in relevant training sessions Eligibility / Qualifications Educational Qualification Bachelor’s degree in any discipline (science or life sciences preferred) Relevant Courses: Pharmacy, Life Sciences, Biotechnology, Microbiology, Biochemistry, Clinical Research, Healthcare Management, Business Administration Experience Requirements Direct experience in the pharmaceutical or life sciences industry 1 to 3 years of experience in event management, medical affairs operations, or commercial support roles preferred Hands-on experience with CRM platforms such as 1CRM or Veeva Vault Proficiency in MS Office applications Key Skills & Competencies Strong project management and organizational skills Excellent written and spoken English communication Solid understanding of medical affairs processes and compliance requirements Event management knowledge within a regulated healthcare environment Financial awareness related to event budgeting and execution Ability to collaborate across multicultural and global teams Digital literacy with an innovative and agile mindset High attention to detail and strong accountability Location & Salary Job Location: Hyderabad, Telangana, India Job Type: Permanent, Full Time Travel Requirement: Travel may be required based on business needs Application Process Eligible candidates can apply online through Sanofi’s official careers portal using the link below: 👉 Apply Online: https://jobs.sanofi.com/en/job/-/-/2649/34364660032 Candidates are encouraged to apply early, as applications may be reviewed on a rolling basis. Frequently Asked Questions (FAQs) Q1: Who is eligible for the Project Specialist – Medical Affairs role? Candidates with a bachelor’s degree and experience in pharma, life sciences, or healthcare operations can apply. Q2: Is prior medical affairs experience mandatory? Direct medical affairs experience is preferred but not mandatory. Event management and CRM experience are critical. Q3: Which CRM systems are used in this role? The role primarily uses the 1CRM events portal and tools like Veeva Vault. Q4: Does this role involve travel? Yes, travel may be required depending on business and event needs. Q5: How do I apply for this Sanofi job in Hyderabad? Applications must be submitted online through Sanofi’s official careers portal. Job Summary Table Company Sanofi Vacancies Project Specialist – Medical Affairs Required Education Bachelor’s Degree, Pharmacy, Life Sciences, Biotechnology Experience 1–3 years Pharma / Life Sciences Event or Medical Affairs Experience [...] Read more...

TransPerfect hiring Project Coordinator Pharmacovigilance

January 23, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Project Coordinator PV Vacancy – Pune TransPerfect hiring Project Coordinator Pharmacovigilance in Pune. Bachelor degree eligible. Full-time on-site vacancy. Apply now. TransPerfect is inviting applications for the role of Project Coordinator – Pharmacovigilance (PV) Solutions at its Pune location. This opportunity is ideal for graduates seeking to build a stable and long-term career in pharmacovigilance, drug safety operations, and healthcare project management. The role offers hands-on exposure to literature monitoring projects, global healthcare clients, and regulatory-driven workflows within a structured professional environment. Company Overview TransPerfect is a globally established provider of language, technology, and business solutions, supporting leading pharmaceutical, biotechnology, clinical research, and healthcare organizations worldwide. The company plays a key role in regulatory submissions, pharmacovigilance services, clinical documentation, and post-marketing safety operations. With a strong reputation in pharmacovigilance and life sciences solutions, TransPerfect supports global drug safety activities by ensuring accuracy, compliance, and operational excellence. The organization follows international regulatory standards and Good Pharmacovigilance Practices, making it a trusted partner for healthcare and pharmaceutical companies. Job Role & Responsibilities The Project Coordinator, Pharmacovigilance (PV) Solutions will handle day-to-day administrative and coordination tasks for literature monitoring and non-linguistic PV projects. The role supports the Production and Project Management teams to ensure timely delivery, compliance with regulatory standards, and consistent service quality. Key Responsibilities Manage administrative components of pharmacovigilance literature monitoring projects Coordinate file transfers, internal tracking, and client deliveries Monitor project timelines and communicate progress to internal stakeholders Ensure strict adherence to client deadlines and quality benchmarks Implement and support Good Pharmacovigilance Practices (GVP) across projects Maintain Good Documentation Practice (GDP) standards in all project records Perform internal checks and balances to ensure process compliance Collaborate with cross-functional teams to resolve project-related issues Complete additional responsibilities assigned by managers or supervisors This role contributes directly to global drug safety and regulatory compliance by supporting accurate and timely pharmacovigilance operations. Eligibility / Qualifications Required Qualifications Minimum Bachelor’s degree in any discipline Strong written and spoken English communication skills Proficiency in Microsoft Word, Excel, and Outlook Ability to adapt and work across multiple technology platforms Strong problem-solving and critical-thinking skills High attention to detail for regulatory-compliant deliverables Excellent organizational and time-management abilities Desired Skills and Experience Ability to multitask in a fast-paced pharmacovigilance environment Comfortable working with global and cross-cultural teams Strong interpersonal and professional communication skills Ability to work independently and collaboratively Proactive mindset with a commitment to service quality Relevant Educational Background B.Pharmacy, M.Pharmacy, Pharm.D, B.Sc Life Sciences, B.Sc Biotechnology, B.Sc Microbiology, B.Sc Biochemistry, B.Sc Chemistry, B.Sc Nursing, M.Sc Life Sciences, M.Sc Biotechnology, M.Sc Pharmacology, Bachelor’s Degree in Science, Pharmacy, Life Sciences, Healthcare Management Location & Salary Job Location: Pune, Maharashtra (On-site) Employment Type: Full-time, Permanent Department: Project Management – Pharmacovigilance Solutions Salary: As per industry standards and candidate experience Compensation is competitive and aligned with current pharmacovigilance and healthcare project management market benchmarks. Application Process Eligible candidates can apply online through the official TransPerfect careers portal using the link below: Apply here: https://transperfect.recruitee.com/o/project-coordinator-pharmacovigilance-pv-solutions-pune Candidates are encouraged to apply early, as applications are reviewed on a rolling basis. Frequently Asked Questions (FAQs) Is this role suitable for freshers? Yes. Graduates with strong communication skills and interest in pharmacovigilance or healthcare project coordination can apply. Is this a work-from-home position? No. This is a full-time on-site role based in Pune. Does this role require pharmacovigilance experience? Prior pharmacovigilance experience is not mandatory, but knowledge of life sciences or healthcare processes is an advantage. What type of projects will I work on? You will support pharmacovigilance literature monitoring and non-linguistic PV projects for global healthcare clients. How do I apply for this job? Applications must be submitted through the official TransPerfect careers portal using the provided link Summary Table Category Details Company TransPerfect Vacancies Project Coordinator – Pharmacovigilance (PV) Solutions Required Education Bachelor’s Degree, B.Pharmacy, M.Pharmacy, Pharm.D, B.Sc Life Sciences, Biotechnology, Microbiology, Biochemistry, Chemistry, Nursing Experience Freshers and Experienced Candidates [...] Read more...

Sanofi Hiring Pharmacovigilance (PV) & Medical Information Officer

February 18, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Sanofi Hiring Pharmacovigilance (PV) & Medical Information Officer | Pharmacy/Medicine | Lysaker, Norway Sanofi is inviting applications for the position of Pharmacovigilance (PV) and Medical Information Officer in Lysaker, Norway. This is a fixed-term, full-time opportunity (ending May 2027) within the North Europe Market Company Organization (MCO) team. The role sits at the intersection of pharmacovigilance, drug safety, regulatory compliance, and medical information services, supporting chronic and specialty therapeutic areas including diabetes, transplant, immunology, oncology, rare diseases, and vaccines. This position is ideal for pharmacy and medical graduates with pharmaceutical industry experience who want to work in global drug safety, adverse event reporting, regulatory compliance, and medical information management within a leading R&D-driven biopharma organization. Company Overview entity is an R&D-driven, AI-powered global biopharmaceutical company dedicated to improving patient lives worldwide. With a strong focus on immunoscience, Sanofi develops innovative medicines and vaccines across oncology, rare diseases, neurology, cardiovascular disorders, diabetes, and immunology. The company combines scientific expertise with digital innovation and artificial intelligence to accelerate drug discovery and lifecycle management. Sanofi’s portfolio reaches over 100 million patients annually, supported by robust pharmacovigilance systems, regulatory excellence, and global safety surveillance frameworks. Operating across multiple regions, Sanofi emphasizes ethical compliance, patient safety, regulatory integrity, and inclusive innovation. Job Role & Responsibilities The Pharmacovigilance (PV) and Medical Information Officer will ensure the safety monitoring and compliant reporting of pharmaceutical products while delivering high-quality medical information to healthcare professionals (HCPs), patients, and internal stakeholders. Pharmacovigilance Responsibilities Maintain comprehensive knowledge of company pharmacovigilance procedures, legal requirements, and global safety regulations. Process adverse event reports in accordance with local legislation and internal quality documents. Provide accurate safety information to Health Authorities and relevant stakeholders. Support the Country Safety Head in safety surveillance, risk management, and signal management activities. Manage product alerts and market research program communications with Pharmacovigilance and Health Authorities. Ensure compliance with global safety reporting timelines and regulatory obligations. Medical Information Responsibilities Respond to medical information inquiries from healthcare professionals, patients, and other stakeholders. Provide scientifically accurate, compliant, and balanced responses aligned with approved labeling and company standards. Maintain documentation of medical information activities in compliance with quality and regulatory requirements. Collaborate with internal departments including regulatory affairs, medical affairs, and quality teams. Cross-Functional Collaboration Work closely with third-party partners involved in PV and Medical Information activities. Contribute actively to North Europe Cluster projects and operational initiatives. Ensure accurate documentation and adherence to pharmacovigilance quality systems. This role demands precision, regulatory awareness, strong communication skills, and the ability to operate within structured pharmacovigilance and compliance frameworks. Eligibility & Qualifications Educational Qualification University degree in: Pharmacy, Medicine, Clinical Pharmacology, Biomedical Sciences, Life Sciences, or equivalent medical/healthcare discipline. Experience Prior experience in the pharmaceutical industry or equivalent healthcare setting. Experience in pharmacovigilance, drug safety, medical information, or regulatory compliance preferred. Core Competencies Strong planning and organizational skills. High level of accuracy and attention to detail. Compliance-driven mindset with understanding of regulatory obligations. Ability to manage safety data and medical information requests efficiently. Communication & Language Skills Excellent written and verbal communication skills. Ability to interact professionally with healthcare professionals and patients. Fluency in English and Norwegian (both written and spoken) is mandatory. Technical Skills Strong computer literacy including Microsoft Office tools. Experience working with pharmacovigilance databases and medical information systems preferred. Candidates must demonstrate regulatory awareness, structured documentation capability, and strong collaboration skills. Location & Employment Details Location: Lysaker, Norway Employment Type: Full-Time Contract Type: Fixed-Term (ending May 2027) Department: Pharmacovigilance & Medical Information Application Process Interested candidates can apply directly through Sanofi’s official careers portal using the link below: Apply Here: https://jobs.sanofi.com/en/job/-/-/2649/34335990720 Applicants should highlight their pharmacovigilance experience, adverse event handling exposure, regulatory compliance knowledge, and medical information expertise in their application. Career Growth Opportunities With experience, professionals can advance into roles such as: Senior Pharmacovigilance Officer Drug Safety Manager Risk Management Specialist Medical Information Manager Regulatory Affairs & Safety Lead The increasing global emphasis on drug safety, benefit-risk evaluation, and regulatory intelligence ensures strong long-term career stability in pharmacovigilance and medical affairs. Frequently Asked Questions (FAQs) 1. Is prior pharmacovigilance experience required? Experience in pharmacovigilance or related pharmaceutical roles is preferred but not strictly limited to PV-only backgrounds. 2. Is Norwegian language proficiency mandatory? Yes, fluency in both English and Norwegian is required. 3. Is this a permanent role? No, this is a fixed-term contract ending May 2027. 4. What therapeutic areas are involved? The role supports chronic and specialty areas including diabetes, transplant, immunology, oncology, rare diseases, and vaccines. 5. Does the role involve regulatory reporting? Yes, the position includes handling adverse event reports and supporting regulatory compliance activities. Summary Table Company Sanofi Vacancies Pharmacovigilance (PV) & Medical Information Officer Required Education Pharmacy, Medicine, Biomedical Sciences, Clinical Pharmacology Experience Pharmaceutical industry experience; PV or medical information exposure preferred [...] Read more...

Accenture Hiring Pharmacovigilance Services Specialist

March 7, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Accenture Hiring Pharmacovigilance Services Specialist – Drug Safety Career Opportunity in Bengaluru Accenture is currently recruiting for the role of Pharmacovigilance Services Specialist within its Pharmacovigilance & Drug Safety Surveillance team. The position is based in Bengaluru, India, and is designed for experienced professionals with 5–8 years of pharmacovigilance experience in the pharmaceutical or clinical research industry. This opening provides an excellent opportunity for pharmacy professionals to work in advanced drug safety monitoring, signal detection, and pharmacovigilance operations supporting global pharmaceutical clients. The Pharmacovigilance Services Specialist will lead signal management activities, support safety surveillance programs, and ensure compliance with international regulatory guidelines governing drug safety reporting. For candidates seeking long‑term careers in pharmacovigilance, drug safety surveillance, and regulatory safety compliance, this role offers exposure to global pharmacovigilance systems, advanced safety databases, and international regulatory frameworks used by leading pharmaceutical companies. Company Overview Accenture is a global professional services company known for its expertise in technology, consulting, operations, digital transformation, and cloud services. With more than 784,000 employees worldwide and operations in over 120 countries, Accenture supports organizations across multiple industries including healthcare, pharmaceuticals, finance, technology, and manufacturing. In the life sciences sector, Accenture works closely with pharmaceutical and biotechnology companies to support clinical development, regulatory compliance, pharmacovigilance operations, and healthcare analytics. The organization combines scientific expertise with advanced technology platforms to help pharmaceutical companies improve drug safety monitoring and regulatory reporting processes. Accenture’s pharmacovigilance teams play a crucial role in ensuring medicines remain safe for patients by monitoring adverse events, analyzing safety data, and supporting global safety surveillance programs. Through its advanced technology infrastructure and global delivery model, Accenture helps pharmaceutical companies manage complex pharmacovigilance workflows efficiently. Professionals working at Accenture gain exposure to cutting‑edge digital solutions used in drug safety monitoring, global regulatory reporting systems, and large‑scale healthcare data analytics projects. Job Role & Responsibilities The Pharmacovigilance Services Specialist will support signal detection and safety surveillance activities associated with pharmaceutical products. The role involves analyzing safety information, managing safety reports, and ensuring compliance with pharmacovigilance regulations. Key responsibilities include: Leading signal management activities including literature reviews and signal detection analysis Authoring signal management reports such as SMART (Signal Management and Review Team) reports Managing safety surveillance team meetings and project coordination Ensuring pharmacovigilance activities are completed within agreed timelines and regulatory standards Performing case identification, data entry, and MedDRA coding for safety reports Managing Individual Case Safety Reports (ICSRs) within safety databases Supporting case processing, submission, and follow‑up activities for adverse event reports Reviewing safety data collected from healthcare providers, clinical trials, and spontaneous reports Ensuring compliance with global pharmacovigilance regulations and company SOPs Supporting safety signal detection and risk assessment activities Coordinating with internal pharmacovigilance teams and external stakeholders Managing small teams or project activities depending on project requirements The role is critical in ensuring that adverse drug reactions are identified, evaluated, and reported according to international regulatory guidelines to protect patient safety. Eligibility / Qualifications Candidates applying for this pharmacovigilance job should meet the following educational and professional requirements. Required Education Candidates must hold a degree in pharmacy or related healthcare discipline. Relevant courses include: Bachelor of Pharmacy, Master of Pharmacy, Pharmacology, Clinical Research, Life Sciences, Pharmaceutical Sciences Experience 5–8 years of pharmacovigilance or drug safety experience in pharmaceutical companies, CROs, or healthcare organizations Experience in signal management, safety surveillance, and case processing Required Skills Strong understanding of pharmacovigilance regulations and drug safety processes Experience with MedDRA coding and ICSR case management Knowledge of signal detection and safety surveillance activities Excellent analytical and problem‑solving skills Strong written and verbal communication skills Ability to collaborate with cross‑functional teams Attention to detail when handling clinical safety data Additional Skills Risk management capability Stakeholder collaboration and interpersonal skills Ability to work in rotational shifts when required Location & Salary Job Location: Bengaluru, India The position may require working in rotational shifts depending on project requirements. Salary details have not been publicly disclosed by the company. Compensation typically depends on the candidate’s experience in pharmacovigilance operations, safety data analysis, and regulatory compliance expertise. Application Process Candidates interested in this pharmacovigilance opportunity can apply through the official Accenture careers portal. Apply here: https://www.accenture.com/in-en/careers/jobdetails?id=AIOC-S01630802_en Applicants are advised to apply through the official website to ensure authenticity and avoid recruitment scams. Frequently Asked Questions What does a Pharmacovigilance Services Specialist do? A Pharmacovigilance Services Specialist monitors drug safety data, manages adverse event reports, performs signal detection activities, and ensures compliance with global pharmacovigilance regulations. What qualifications are required for this role? Candidates must have a Bachelor of Pharmacy or Master of Pharmacy degree with relevant pharmacovigilance experience. How much experience is required? Accenture requires approximately 5–8 years of experience in pharmacovigilance or drug safety operations. What skills are important for pharmacovigilance professionals? Key skills include safety data analysis, MedDRA coding, regulatory knowledge, signal detection, communication skills, and attention to detail. How can I apply for this job? Candidates can apply through the official Accenture careers website using the application link provided above. Job Summary Company Accenture Vacancies Pharmacovigilance Services Specialist Required Education Bachelor of Pharmacy, Master of Pharmacy, Pharmacology, Clinical Research, Life Sciences, Pharmaceutical Sciences Experience 5–8 years pharmacovigilance or drug safety experience [...] Read more...

Abbott Pharmacovigilance Hiring PV Specialist

March 6, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Abbott Hiring PV Compliance Specialist – Pharmacovigilance & Drug Safety Job in Mumbai Abbott is currently hiring for the position of PV Compliance Specialist in the Research & Development division. The role is based in Mumbai, India and offers an excellent opportunity for professionals interested in pharmacovigilance, drug safety compliance, and regulatory monitoring within the pharmaceutical industry. This role supports the global pharmacovigilance (PV) compliance monitoring system and focuses on tracking safety metrics, managing corrective and preventive actions (CAPA), and ensuring adherence to global drug safety regulations. Professionals working in this position contribute directly to patient safety by ensuring that pharmacovigilance systems operate according to regulatory requirements and international safety standards. The PV Compliance Specialist works closely with global pharmacovigilance teams, regulatory professionals, and quality management groups to monitor compliance indicators, analyze safety reporting metrics, and ensure that pharmacovigilance processes align with industry regulations. For candidates seeking careers in drug safety, pharmacovigilance operations, compliance monitoring, or pharmaceutical quality systems, this opportunity provides strong exposure to global safety surveillance systems and regulatory frameworks. Company Overview Abbott is a globally recognized healthcare company focused on developing innovative medicines, diagnostic technologies, nutrition products, and medical devices. With a presence in more than 160 countries, Abbott plays a major role in advancing healthcare through research, technology, and scientific innovation. The company’s research and development teams work continuously to improve patient outcomes through the development of safe and effective healthcare solutions. Abbott’s pharmacovigilance and drug safety programs are designed to ensure that medicines and medical devices meet strict regulatory standards and maintain the highest levels of patient safety. Abbott invests heavily in regulatory science, clinical development, safety monitoring, and compliance management. Employees working in pharmacovigilance and regulatory roles contribute to global healthcare safety systems that monitor adverse events, evaluate risk signals, and support regulatory reporting requirements. Professionals joining Abbott gain exposure to international pharmaceutical regulations, safety surveillance systems, and global quality standards used in modern drug development and post‑marketing safety monitoring. Job Role and Responsibilities The PV Compliance Specialist will support the pharmacovigilance compliance monitoring framework and ensure that safety processes meet internal quality standards and regulatory requirements. Key responsibilities include: Collecting compliance data from global pharmacovigilance teams and medical device vigilance systems within agreed timelines Maintaining and enhancing pharmacovigilance compliance tracking systems and databases Supporting development of monitoring tools with assistance from internal IT teams Compiling key pharmacovigilance metrics and preparing compliance monitoring reports Drafting Key Performance Indicator (KPI) reports and pharmacovigilance compliance summaries Requesting non‑compliance details and corrective actions from responsible teams when required Reviewing corrective and preventive action (CAPA) records and ensuring timely follow‑up on quality issues Monitoring trends related to compliance deviations and identifying root causes of recurring issues Initiating investigations into pharmacovigilance compliance deviations and documenting findings Proposing corrective solutions according to established pharmacovigilance processes Coordinating with relevant stakeholders to ensure PV compliance indicators are monitored effectively Supporting training programs for staff on pharmacovigilance compliance processes and CAPA management systems Escalating significant compliance issues to the Head of PV System & Compliance or Qualified Person for Pharmacovigilance (QPPV) when required This role plays an important part in maintaining regulatory compliance within pharmacovigilance systems and ensuring that drug safety monitoring activities remain consistent with global healthcare regulations. Eligibility and Qualifications Candidates applying for this pharmacovigilance and drug safety role should meet the following educational and professional requirements. Required Education A bachelor’s or master’s degree in life sciences, pharmacy, or healthcare-related disciplines. Relevant courses include: Pharmacy, Pharmacology, Clinical Research, Biotechnology, Biochemistry, Microbiology, Life Sciences, Biomedical Sciences, Toxicology, Public Health Experience Experience in pharmacovigilance operations, drug safety monitoring, regulatory compliance, or quality management systems is preferred. Candidates with exposure to pharmacovigilance compliance systems, CAPA processes, or safety reporting frameworks will have an advantage. Required Skills Knowledge of pharmacovigilance systems and drug safety regulations Understanding of CAPA processes and compliance monitoring frameworks Ability to analyze safety metrics and regulatory compliance data Strong attention to detail and documentation accuracy Ability to manage compliance tracking databases and reporting tools Effective communication and collaboration skills Ability to work with cross‑functional regulatory and safety teams Professionals with experience in pharmacovigilance auditing, safety surveillance systems, and regulatory reporting environments are well suited for this role. Location and Salary Job Location: Mumbai, India The position operates within Abbott’s Research & Development and pharmacovigilance compliance environment. Salary details for this position have not been publicly disclosed by the company. Compensation typically varies depending on candidate experience in pharmacovigilance operations, regulatory compliance management, and pharmaceutical safety monitoring. Application Process Candidates interested in this pharmacovigilance job opportunity can apply through the official Abbott careers portal. Apply here: https://www.jobs.abbott/us/en/job/ABLAUS31141459ENUSEXTERNAL/PV-Compliance-Specialist Applicants should apply only through the official company website to ensure authenticity and avoid recruitment scams. Frequently Asked Questions What does a PV Compliance Specialist do? A PV Compliance Specialist monitors pharmacovigilance compliance systems, tracks safety reporting metrics, reviews CAPA processes, and ensures drug safety activities follow regulatory guidelines. What qualifications are required for this role? Candidates typically require a degree in life sciences, pharmacy, pharmacology, biotechnology, or related healthcare fields. Is pharmacovigilance experience required? Experience in pharmacovigilance operations, drug safety monitoring, or compliance management is generally preferred for this role. What skills are important for pharmacovigilance compliance roles? Key skills include regulatory knowledge, compliance monitoring, CAPA management, data analysis, documentation accuracy, and collaboration with safety and regulatory teams. How can I apply for this job? Candidates can apply through the official Abbott careers website using the application link provided above. Job Summary Company Abbott Vacancies PV Compliance Specialist Required Education Pharmacy, Pharmacology, Clinical Research, Biotechnology, Biochemistry, Microbiology, Life Sciences, Biomedical Sciences, Toxicology, Public Health Experience Pharmacovigilance, drug safety, or regulatory compliance experience preferred [...] Read more...

Accenture Fresher Pharmacovigilance Vacancies – PV Services Associate in Chennai

March 6, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Accenture Hiring Pharmacovigilance Services Associate – Drug Safety & ICSR Processing | 0–2 Years | Bengaluru Accenture is hiring Pharmacovigilance Services Associates for its Pharmacovigilance Operations team in Bengaluru. This is a full-time opportunity for freshers and early-career professionals with 0–2 years of experience in drug safety, adverse event reporting, or clinical safety operations. Candidates with qualifications in BAMS, Bachelor’s Degree in Life Sciences, or Master’s Degree in Life Sciences are eligible to apply. This role focuses on pharmacovigilance case processing, global safety database management, ICSR handling, and regulatory compliance in accordance with global drug safety guidelines. If you are looking to build a long-term career in pharmacovigilance, drug safety surveillance, and regulatory operations within a global organization, this position offers structured learning and exposure to international safety standards. Company Overview Accenture is a global professional services company with expertise in digital transformation, cloud solutions, technology services, and intelligent operations. With over 784,000 employees serving clients in more than 120 countries, Accenture supports organizations across healthcare, life sciences, pharmaceuticals, and biotechnology sectors. Within the life sciences and healthcare vertical, Accenture provides pharmacovigilance services, regulatory support, clinical data management, and safety operations solutions to leading pharmaceutical companies worldwide. The organization combines domain knowledge with advanced technology platforms to ensure regulatory compliance and patient safety. Working at Accenture means being part of large-scale global drug safety projects that directly support public health and regulatory reporting obligations. Job Role & Responsibilities The Pharmacovigilance Services Associate is responsible for end-to-end case processing and management of Individual Case Safety Reports (ICSRs) within global safety databases. Core Responsibilities Identify and create safety cases in the global safety database from intake workflows, client mailboxes, electronic gateways, and other sources. Perform triage, prioritization, and validation of adverse event reports. Process serious and non-serious cases (AEs, SAEs, SUSARs) as per client SOPs and global regulatory timelines. Conduct duplicate checks and validate minimum safety information. Perform medical coding using MedDRA and WHO-Drug dictionaries. Draft case narratives and assess seriousness and causality in collaboration with medical reviewers. Submit cases within required regulatory timelines and monitor submission acknowledgments. Retrieve and reconcile safety information from portals such as EVWEB and MHRA. Request follow-ups for missing or incomplete safety data. Perform translations of source documents and safety narratives when required. Support audits, inspections, and compliance reviews. Archive all case-related communications within the safety database. This role demands precision, regulatory awareness, and strong knowledge of pharmacovigilance workflows to ensure compliance with global health authority requirements. Eligibility / Qualifications Educational Qualification Bachelor of Ayurvedic Medicine and Surgery (BAMS), Bachelor’s Degree in Life Sciences, or Master’s Degree in Life Sciences. Relevant Courses: BAMS, B.Pharm, M.Pharm, BSc Life Sciences, MSc Life Sciences, Biotechnology, Microbiology, Biochemistry, Pharmacology, Clinical Research, Biomedical Sciences. Experience 0–2 years of experience in pharmacovigilance, drug safety, healthcare, or clinical research operations. Freshers with strong pharmacovigilance knowledge may be considered. Required Skills Good understanding of pharmacovigilance and drug safety surveillance. Knowledge of ICH guidelines and global regulatory reporting requirements. Familiarity with MedDRA and WHO-Drug coding dictionaries. Experience or knowledge of safety databases. Strong medical writing and documentation skills. Excellent English communication skills (written and spoken). Ability to manage timelines and prioritize cases effectively. Proficiency in MS Office tools. Candidates who demonstrate accuracy in adverse event evaluation and compliance with regulatory timelines will perform strongly in this role. Location & Employment Details Location: Bengaluru, India Job Type: Full-Time Experience Level: 0–2 Years Job Number: AIOC-S01621720 Salary details are not publicly disclosed. Compensation is aligned with industry standards for entry-level pharmacovigilance and drug safety professionals. Why This Role Is Important in Drug Safety Pharmacovigilance plays a critical role in monitoring the safety of medicines after they are marketed. Accurate evaluation and reporting of adverse events ensure regulatory compliance and protect patient health worldwide. The Pharmacovigilance Services Associate contributes directly to global drug safety surveillance by processing ICSRs, ensuring timely submissions, and maintaining data integrity within global safety systems. This function supports pharmaceutical companies in meeting strict compliance standards set by health authorities. For candidates seeking a stable and high-growth career in pharmacovigilance operations, regulatory affairs, or clinical safety, this role offers foundational experience and global exposure. Application Process Interested candidates can apply directly through the official Accenture career portal using the link below: Apply Here: https://www.accenture.com/in-en/careers/jobdetails?id=AIOC-S01621720_en&title=Pharmacovigilance+Services+Associate Ensure your resume highlights knowledge of adverse event reporting, medical terminology, regulatory guidelines, and safety database exposure. Frequently Asked Questions (FAQs) 1. Who can apply for this Pharmacovigilance role at Accenture? Candidates with BAMS, Bachelor’s or Master’s degree in Life Sciences and up to 2 years of relevant experience can apply. 2. Is this role suitable for freshers? Yes. Freshers with strong pharmacovigilance knowledge are eligible. 3. What databases or tools should candidates know? Familiarity with global safety databases, MedDRA, WHO-Drug coding, and MS Office tools is preferred. 4. What types of cases will be handled? The role includes processing AEs, SAEs, SUSARs, and other Individual Case Safety Reports. 5. What career growth opportunities are available? Professionals can progress to Senior Drug Safety Associate, Pharmacovigilance Specialist, Safety Scientist, or Regulatory Operations roles. Recruitment Summary Company Accenture Vacancies Pharmacovigilance Services Associate Required Education BAMS / Bachelor’s or Master’s in Life Sciences Experience 0–2 Years in Pharmacovigilance or Drug Safety [...] Read more...

Syneos Health – Pharmacovigilance Safety & Pv Specialist I Openings

March 4, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Syneos Health Hiring Safety & Pharmacovigilance Specialist I – B.Pharm / M.Pharm / PharmD | Gurugram & Hyderabad Syneos Health is currently recruiting for the position of Safety & Pharmacovigilance (PV) Specialist I within its global drug safety and pharmacovigilance operations team. This full‑time onsite opportunity is available in Gurugram and Hyderabad, India and is designed for professionals with at least 2 years of pharmacovigilance or drug safety experience. The vacancy falls under the Pharmacovigilance and Drug Safety department, where professionals contribute to adverse event case processing, safety database management, and regulatory safety reporting for clinical trials and post‑marketing surveillance programs. Candidates with qualifications such as B.Pharm, M.Pharm, PharmD, or BDS and experience in ICSR case processing, drug safety databases, MedDRA coding, and clinical trial safety monitoring are ideal for this role. Professionals working in CROs, pharmaceutical companies, or drug safety outsourcing organizations will find this opportunity aligned with long‑term career growth in pharmacovigilance and regulatory drug safety. This role allows professionals to work with global clinical development teams while contributing to safety monitoring activities that support the development and commercialization of new medicines worldwide. Company Overview Syneos Health is a leading global biopharmaceutical solutions organization that integrates clinical development, medical affairs, and commercialization services. The company collaborates with pharmaceutical, biotechnology, and healthcare organizations to accelerate the development and delivery of innovative therapies to patients worldwide. With more than 29,000 employees across 110 countries, Syneos Health provides comprehensive support throughout the drug development lifecycle—from early clinical trials to post‑marketing safety surveillance. Over the past five years, Syneos Health has contributed to the development of 94% of newly approved FDA drugs and 95% of EMA‑authorized medicines, demonstrating its strong influence in global clinical research and pharmacovigilance operations. The organization focuses on patient‑centric clinical development models and uses advanced analytics, medical expertise, and operational excellence to ensure safe and effective therapies reach patients faster. Job Role & Responsibilities The Safety & PV Specialist I is responsible for supporting pharmacovigilance activities related to adverse event reporting, safety database management, and regulatory compliance across clinical trials and post‑marketing programs. Pharmacovigilance Case Processing Perform Individual Case Safety Report (ICSR) processing in accordance with sponsor requirements and regulatory guidelines. Enter and validate safety information within pharmacovigilance safety databases. Perform MedDRA coding for adverse events, medical history, medications, and laboratory data. Evaluate case information for completeness, regulatory reportability, and accuracy. Safety Data Management Maintain safety tracking systems and ensure accurate case processing timelines. Identify duplicate safety reports and manage reconciliation activities. Conduct literature screening for drug safety information. Perform medical coding and maintain drug dictionaries used for safety reporting. Regulatory Compliance & Reporting Support the preparation and submission of expedited safety reports according to global regulatory requirements. Assist in the validation and submission of xEVMPD product records. Participate in activities related to SPOR and IDMP regulatory frameworks. Ensure compliance with ICH‑GCP, GVP guidelines, and global pharmacovigilance regulations. Quality & Documentation Activities Conduct quality review of ICSRs to maintain high safety data standards. Ensure all pharmacovigilance documentation is properly maintained within the Trial Master File (TMF). Participate in audits and inspections when required. Cross‑Functional Collaboration Work with safety physicians, pharmacovigilance teams, and clinical operations staff. Maintain professional communication with internal and external stakeholders. Contribute to team discussions regarding safety trends and risk management activities. Eligibility / Qualifications Educational Qualification Candidates must hold a degree in pharmacy, healthcare, or life sciences. Relevant Courses: B.Pharm, M.Pharm, PharmD, BDS, BSc Life Sciences, MSc Life Sciences, Biotechnology, Microbiology, Biochemistry, Clinical Research, Pharmacology. Experience Minimum 2 years of pharmacovigilance or drug safety experience. Experience in clinical trial safety case processing or literature case processing is preferred. Required Skills Knowledge of ICSR processing and pharmacovigilance workflows. Familiarity with safety databases and drug safety reporting systems. Understanding of ICH‑GCP, GVP guidelines, and drug development processes. Experience with MedDRA coding and medical terminology. Strong attention to detail and analytical skills. Proficiency in Microsoft Office (Word, Excel, PowerPoint). Strong written and verbal communication abilities. Professionals who can manage safety case timelines, maintain accuracy, and ensure regulatory compliance will succeed in this position. Location & Salary Job Locations: Gurugram, Haryana and Hyderabad, Telangana – India Employment Type: Full‑Time Onsite Salary information has not been publicly disclosed. Compensation will align with industry standards for pharmacovigilance professionals working in global CRO organizations. Application Process Interested candidates can apply directly through the official Syneos Health careers portal using the link below: Apply Here: https://syneoshealth.wd12.myworkdayjobs.com/Syneos_Health_External_Site/job/IND-Gurugram/Safety—PV-Specialist-I–Gurugram-Hyderabad-_25104799-1/apply Ensure that your resume highlights experience in pharmacovigilance case processing, safety databases, regulatory drug safety, and MedDRA coding. Frequently Asked Questions (FAQs) 1. Who can apply for the Safety & PV Specialist role at Syneos Health? Candidates with degrees such as B.Pharm, M.Pharm, PharmD, or BDS and at least two years of pharmacovigilance experience can apply. 2. Is pharmacovigilance experience mandatory? Yes. Applicants must have a minimum of two years of relevant drug safety or pharmacovigilance experience. 3. What type of organization is Syneos Health? Syneos Health is a global contract research and biopharmaceutical services company supporting drug development, clinical trials, and pharmacovigilance operations. 4. What career opportunities exist after this role? Professionals can advance to Senior PV Specialist, Drug Safety Associate, Safety Scientist, or Pharmacovigilance Manager roles. 5. What regulatory guidelines are important for this job? Knowledge of ICH‑GCP, GVP guidelines, and global pharmacovigilance regulations is important for performing safety reporting tasks. Recruitment Summary Company Syneos Health Vacancies Safety & PV Specialist I Required Education B.Pharm, M.Pharm, PharmD, BDS or Life Sciences Experience Minimum 2 Years Pharmacovigilance / Drug Safety Experience [...] Read more...

Qinecsa Solutions Hiring Pharmacovigilance MICC Jobs for Life Sciences Graduates

March 3, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now MICC Jobs for Life Sciences Graduates | Qinecsa Solutions Bangalore Hiring Qinecsa Solutions is hiring MICC (Medical Information Contact Center) Professionals with 1–2 years of experience in Bangalore. Apply now to advance your healthcare communication career. Be the Voice of Global Healthcare – Join Qinecsa’s MICC Team Are you a Life Sciences graduate with a passion for healthcare communication? Qinecsa Solutions, a global leader in pharmacovigilance and medical communication services, is expanding its Bangalore team. We’re currently hiring MICC (Medical Information Contact Center) Professionals who want to contribute to improving global patient outcomes. Located in Bangalore, this full-time, office-based position offers the chance to work alongside a team that supports pharmaceutical leaders through safety, science, and digital innovation. Why Choose Qinecsa Solutions? Innovation Meets Impact Qinecsa is known for its comprehensive safety services and commitment to data-driven decision-making in life sciences. With cutting-edge technology and a robust regulatory approach, Qinecsa offers an ideal environment for healthcare professionals looking to grow. MICC Role Overview Key Responsibilities: Respond to medical information inquiries from healthcare professionals and patients Manage safety-related communication and documentation Ensure timely and accurate responses while adhering to regulatory requirements Collaborate with cross-functional teams to escalate complex issues Maintain compliance with company and industry standards Required Skills: Excellent English communication and interpersonal skills Familiarity with safety reporting and healthcare regulations Quick adaptability in a fast-paced, regulated setting Proficiency in medical writing or documentation (preferred) Who Can Apply? Candidates from the following educational backgrounds are encouraged to apply: Bachelor of Pharmacy (BPharm) Doctor of Pharmacy (PharmD) Bachelor of Medicine and Bachelor of Surgery (MBBS) Bachelor of Science in Nursing (BSc Nursing) Other relevant Life Sciences degrees Experience Required: 1 to 2 years in a Medical Information Contact Center or similar setting. How to Apply Location: Bangalore (Office-based role) Email to Apply: Nithin.Vijendra@Qinecsa.com Send your updated CV to the above email. Shortlisted candidates will be contacted for the interview process. About Qinecsa Solutions Qinecsa Solutions is a trusted global partner for pharmacovigilance, medical writing, and healthcare communication services. By integrating safety, science, and digital technologies, Qinecsa plays a crucial role in enhancing patient safety and supporting regulatory excellence across the pharmaceutical industry. Joining Qinecsa means becoming part of an innovative, growth-oriented organization focused on better outcomes in global healthcare. Summary Table Company Name Current Vacancies in Departments Qinecsa Solutions Medical Information Contact Center (MICC) Required Education Experience Required BPharm, PharmD, MBBS, BSc Nursing, Life Sciences Degrees 1–2 years [...] Read more...

Vizen Life Sciences Hiring Drug Safety Associate & Drug Safety Physician | Pharmacovigilance Jobs

March 3, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Vizen Life Sciences Hiring Drug Safety Associate & Drug Safety Physician | Pharmacovigilance Jobs | Immediate Joiners Vizen Life Sciences is currently hiring for multiple positions in its Pharmacovigilance and Drug Safety department. The open roles include Drug Safety Associate (2–8 years experience) and Drug Safety Physician (MBBS/BDS qualified). These positions are ideal for professionals with mandatory pharmacovigilance experience who are ready to join immediately and contribute to global drug safety operations. As regulatory scrutiny around drug safety, adverse event reporting, and risk management continues to increase globally, experienced pharmacovigilance professionals are in strong demand. These roles provide exposure to safety data management, medical review, signal detection, and regulatory compliance aligned with international health authority standards. Company Overview Vizen Life Sciences operates in the life sciences and healthcare services domain, supporting pharmaceutical, biotechnology, and medical device companies in ensuring regulatory compliance and patient safety. The organization focuses on pharmacovigilance, drug safety monitoring, regulatory documentation, and risk management services. Drug safety functions are critical in protecting patient health and maintaining compliance with global regulatory authorities such as the US FDA, EMA, MHRA, and other international agencies. Through structured safety reporting systems and medical evaluation processes, Vizen Life Sciences contributes to strengthening post-marketing surveillance and risk mitigation strategies for marketed and investigational products. Professionals joining the organization gain hands-on exposure to global safety databases, aggregate reporting, regulatory timelines, and quality-driven pharmacovigilance systems. Job Role & Responsibilities Drug Safety Associate (2–8 Years Experience) The Drug Safety Associate will be responsible for managing day-to-day pharmacovigilance activities and ensuring compliance with global drug safety regulations. Key Responsibilities: Processing and reviewing Individual Case Safety Reports (ICSRs). Performing case triage, data entry, coding (MedDRA/WHO-DD), and medical assessment support. Conducting follow-ups for incomplete safety information. Supporting aggregate report preparation where applicable. Ensuring compliance with global pharmacovigilance regulations and client SOPs. Maintaining accurate documentation within safety databases. Supporting audit and inspection readiness. Candidates must have hands-on pharmacovigilance experience and strong understanding of adverse event reporting workflows. Drug Safety Physician (MBBS/BDS) The Drug Safety Physician will play a critical role in medical review, signal detection, and benefit-risk evaluation activities. Key Responsibilities: Medical review and assessment of Individual Case Safety Reports. Causality assessment and narrative writing. Evaluation of serious adverse events and medically significant cases. Contribution to signal detection and risk management activities. Supporting aggregate safety report review (PSUR, PBRER, DSUR, etc.). Providing medical input for regulatory submissions and health authority responses. Ensuring compliance with ICH guidelines and global pharmacovigilance standards. This position requires strong clinical judgment, analytical thinking, and regulatory awareness. Eligibility / Qualifications Drug Safety Associate Educational Qualification: B.Pharm, M.Pharm, PharmD, MSc Life Sciences, MSc Pharmacology, MSc Biotechnology, or related healthcare qualification. Experience: 2–8 years of pharmacovigilance experience. Experience in ICSR processing and safety database management. Understanding of global regulatory reporting requirements. Drug Safety Physician Educational Qualification: MBBS, BDS (Completed and registered). Experience: Pharmacovigilance experience is mandatory. Experience in medical review, case assessment, and regulatory safety documentation preferred. Key Skills Required Strong knowledge of pharmacovigilance processes and global safety regulations. Familiarity with ICH guidelines and adverse event reporting standards. Attention to detail and high-quality documentation practices. Ability to manage timelines and multiple case workflows. Strong communication and analytical skills. Experience working with safety databases and regulatory compliance systems. Location & Employment Details Employment Type: Full-time Joining: Immediate joiners preferred Department: Pharmacovigilance / Drug Safety Salary details are not disclosed publicly. Compensation is aligned with industry standards for drug safety and pharmacovigilance professionals based on experience and qualification. Application Process Interested and eligible candidates can submit their updated CV to: Email: careers@vizenlifesciences.com Applicants are advised to clearly mention the position applied for (Drug Safety Associate or Drug Safety Physician) in the subject line of the email and highlight relevant pharmacovigilance experience. Frequently Asked Questions (FAQs) 1. Is pharmacovigilance experience mandatory? Yes. Prior pharmacovigilance experience is mandatory for both roles. 2. Are freshers eligible? No. Only candidates with relevant drug safety experience will be considered. 3. What qualifications are required for the Drug Safety Physician role? Candidates must hold MBBS or BDS qualification with pharmacovigilance exposure. 4. What experience range is required for Drug Safety Associate? Candidates with 2 to 8 years of pharmacovigilance experience are eligible. 5. Are immediate joiners preferred? Yes. Immediate joiners will be given preference. Summary Company Vizen Life Sciences Vacancies Drug Safety Associate; Drug Safety Physician Required Education B.Pharm, M.Pharm, PharmD, MSc Life Sciences, MBBS, BDS Experience 2–8 Years (Associate); PV Experience Mandatory (Physician) [...] Read more...

Amgen Pharmacovigilance Hiring Case Management – Specialist (Device Safety)

March 3, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Amgen Hiring Case Management – Specialist (Device Safety) | Life Sciences | Hyderabad Amgen is hiring for the position of Case Management – Specialist (Device Safety) at its Hyderabad, India location. This is an on-site role within the Pharmacovigilance and Drug Safety function, supporting global device and combination product safety operations. The opportunity is suited for experienced professionals in drug safety, pharmacovigilance, life sciences, or medical device safety who meet the required academic and experience criteria. If you are looking for pharmacovigilance jobs in Hyderabad, drug safety specialist roles in biotech, or ICSR case processing careers in global regulatory environments, this position offers exposure to FDA, EMA, and worldwide regulatory reporting within a leading biotechnology company. Company Overview Amgen is one of the world’s pioneering biotechnology companies, founded in 1980 with a clear mission to serve patients living with serious illnesses. With a strong presence across Oncology, Inflammation, General Medicine, and Rare Diseases, Amgen develops and delivers innovative biologic therapies that reach millions of patients globally. The company operates in highly regulated international markets and maintains strict compliance with global pharmacovigilance regulations, Good Manufacturing Practices (GMP), and Good Pharmacovigilance Practices (GVP). Amgen’s culture is science-driven, collaborative, and grounded in strong ethical standards. Employees contribute directly to advancing biotechnology innovation while ensuring patient safety remains the top priority. The Device Safety and Case Management team plays a critical role in monitoring adverse events, ensuring regulatory reporting compliance, and maintaining inspection readiness across global health authorities. Job Role & Responsibilities The Case Management – Specialist (Device Safety) will be accountable for the quality and compliance of Individual Case Safety Reports (ICSRs) related to device and combination products for both clinical trial and post-market cases. Key Responsibilities Oversee global processing of device and combination product ICSRs. Ensure high-quality case intake, review, and submission in compliance with FDA, EMA, and other regulatory authority requirements. Act as US/EU local safety office contact point for regulatory reporting. Submit Individual Case Safety Reports to health authorities, license partners, and vendors. Monitor vendor performance, analyze quality metrics, and identify trends in case processing. Ensure vendor compliance with approved pharmacovigilance processes and training requirements. Support audit readiness and external regulatory inspections. Undertake delegated activities from the Qualified Person for Pharmacovigilance (QPPV) as outlined in the PV System Master File. Assist with Periodic Aggregate Safety Reports (PASR) and lifecycle safety reporting activities when applicable. Operational & Compliance Activities Work within Amgen’s Quality Management System framework. Ensure timely reporting and regulatory compliance for device safety cases. Implement Standard Operating Procedures (SOPs) for pharmacovigilance case management. Contribute to system improvements and process enhancements related to case intake. Maintain quality of Product Complaints (PC), Adverse Event (AE), and other safety records. Apply analytical skills to assess moderately complex safety cases across multiple systems. This role demands strong regulatory awareness, attention to detail, and the ability to manage strict reporting timelines. Accurate case processing directly impacts patient safety, regulatory compliance, and global product integrity. Eligibility & Qualifications Amgen is seeking highly experienced professionals with a strong academic background and substantial exposure to drug safety or life sciences functions. Basic Qualification Criteria One of the following combinations is required: Doctorate degree with 4 years of Drug Safety or Life Sciences experience OR Master’s degree with 7 years of Drug Safety or Life Sciences experience OR Bachelor’s degree with 9 years of Drug Safety or Life Sciences experience Preferred Education Background Bachelor’s or higher degree in health-care or scientific disciplines such as: B.Pharm, M.Pharm, Pharm.D, MBBS, BDS, BSc Nursing, MSc Nursing, BSc Life Sciences, MSc Life Sciences, Biotechnology, Microbiology, Biochemistry, Biomedical Sciences, or related clinical and pharmaceutical sciences fields. Preferred Experience Experience in Pharmacovigilance or Quality within biotech, pharmaceutical, or medical device industries. Hands-on exposure to safety databases or corporate intake systems. Familiarity with global safety reporting regulations. Experience supporting audits and regulatory inspections. Required Skills & Competencies Strong understanding of Good Pharmacovigilance Practices (GVP) and Good Manufacturing Practices (GMP). Familiarity with clinical development processes. High case-level productivity and quality standards. Strong analytical and documentation skills. Ability to work in a matrixed team environment. Proficiency in Microsoft Office tools including Word, Excel, PowerPoint, Project, and Outlook. Ability to manage strict timelines and deliver high-quality results consistently. Location & Salary Location: Hyderabad, India Work Model: On-Site Department: Pharmacovigilance / Device Safety / Case Management Job ID: R-236207 Amgen offers competitive compensation aligned with industry standards for senior pharmacovigilance and drug safety professionals in India. In addition to base salary, employees receive comprehensive total rewards, benefits, and career development support. The organization emphasizes professional growth, collaborative teamwork, and a supportive work environment focused on scientific excellence and patient safety. Application Process Interested candidates can apply directly through Amgen’s official career portal using the link below: Apply Here: https://careers.amgen.com/en/job/-/-/87/91610855360 Application Tips Clearly mention experience in ICSR processing and safety reporting. Highlight exposure to FDA, EMA, or global regulatory submissions. Include audit or inspection support experience if applicable. Detail experience with pharmacovigilance databases and vendor oversight. Shortlisted candidates will be contacted for further evaluation. Frequently Asked Questions (FAQs) 1. Is this role suitable for freshers? No. This role requires significant experience in drug safety or life sciences. 2. Is pharmacovigilance experience mandatory? Yes. Experience in drug safety, pharmacovigilance, or related quality functions is essential. 3. What type of reports will be handled? The role involves Individual Case Safety Reports (ICSRs) and may support Periodic Aggregate Safety Reports (PASR). 4. Is this role regulatory-facing? Yes. The specialist interacts with regulatory authorities such as FDA and EMA for safety reporting. 5. Is this a global role? Yes. The position supports global device and combination product case management. 6. What career growth can be expected? Professionals can advance to Senior Safety Specialist, Safety Manager, Global PV Lead, or Regulatory Safety Leadership roles. Company Amgen Vacancies Case Management – Specialist (Device Safety) Required Education Doctorate, Master’s, or Bachelor’s degree in Life Sciences, Pharmacy, Medicine, Biotechnology, Nursing or related healthcare/scientific fields Experience 4–9+ years in Drug Safety, Pharmacovigilance, or Life Sciences (as per qualification criteria) [...] Read more...

Parexel Fresher Pharmacovigilance Hiring | Patient Safety Associate

March 2, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Patient Safety Associate Fresher – Hyderabad MPharm/PharmD/BDS freshers required for Patient Safety Associate I vacancies at Parexel, Hyderabad/Mohali. Patient safety and pharmacovigilance are core pillars of modern drug development, ensuring that medicines are continuously monitored for safety throughout their lifecycle. Parexel is currently hiring Patient Safety Associate I professionals for its Hyderabad and Mohali offices. This entry-level opportunity is designed specifically for fresh graduates who want to start their careers in pharmacovigilance, drug safety operations, and global regulatory compliance within a leading clinical research organization. Company Overview Parexel is a globally recognized clinical research organization providing end-to-end clinical development solutions to pharmaceutical, biotechnology, and medical device companies. From early-phase clinical trials to regulatory submissions and post-marketing safety surveillance, Parexel supports the full development lifecycle of innovative therapies. Driven by a patient-first philosophy, Parexel combines scientific expertise, regulatory knowledge, and operational excellence to help sponsors bring safe and effective treatments to patients worldwide. With operations across multiple regions, Parexel is known for its strong ethical culture, quality-driven processes, and deep commitment to improving global health outcomes. Job Role & Responsibilities The Patient Safety Associate I role is a full-time, office-based contractual position focused on Individual Case Safety Report processing, safety reporting, literature surveillance, and regulatory compliance activities. General Pharmacovigilance Responsibilities • Develop foundational knowledge of product safety profiles, labeling, and global pharmacovigilance regulations • Follow project-specific workflows, standard operating procedures, and reporting timelines • Support compliance with global regulatory reporting requirements • Assist in preparation for audits and inspections under supervision • Participate in internal and client-specific training programs through the Learning Management System • Ensure timely and accurate completion of timesheets and documentation ICSR Processing & Case Management • Monitor incoming safety reports from sources such as safety mailboxes, EudraVigilance, and literature databases • Perform triage of incoming reports for completeness, validity, and legibility • Enter valid cases into safety databases following client conventions and SOPs • Create cases, perform data entry, and advance cases through workflow stages • Prepare Adverse Drug Reaction forms and medically cohesive case narratives • Perform MedDRA coding in line with term selection guidelines • Assess seriousness, causality, and expectedness of adverse events • Request follow-ups and manage queries related to incomplete safety information • Perform quality and validation checks on processed cases Safety Reporting & Submissions • Submit Individual Case Safety Reports and periodic safety reports to health authorities and ethics committees • Support expedited and aggregate safety reporting activities • Maintain reporting schedules and support on-time submission compliance • Perform unblinding of treatment codes for safety reporting when required • Prepare and file project documentation in electronic document management systems • Support audits, inspections, and regulatory interactions as designated Literature Surveillance & Signal Support • Conduct literature searches based on approved search strategies • Screen scientific publications for potential adverse drug reactions and safety signals • Prepare and review literature abstracts and summaries • Support signal detection activities by flagging relevant safety findings • Maintain local journal lists and update search strategies as required Affiliate & Regulatory Support Activities • Support communication between global safety teams and local affiliates • Assist with regulatory applications, registrations, and lifecycle updates • Support electronic reporting registrations and portal setup for sponsors • Assist with data reconciliation, compliance metrics, and follow-up activities • Maintain regulatory intelligence trackers and safety reporting databases Eligibility / Qualifications This role is designed for recent graduates seeking entry-level pharmacovigilance jobs. Required qualifications: • MPharm, PharmD, or BDS • Year of passing: 2025 • Basic understanding of pharmacovigilance and drug safety concepts • Strong written and verbal communication skills • Willingness to work in an office-based environment • Ability to learn global regulations including ICH guidelines Relevant educational background includes: MPharm, PharmD, BDS, MSc Pharmacology, MSc Clinical Research, Biotechnology, Microbiology, Biochemistry No prior pharmacovigilance experience is mandatory, making this an ideal fresher pharmacovigilance role. Location & Salary Job Location: Hyderabad or Mohali This is a full-time, office-based role offered on a one-year contractual basis. Salary details are not publicly disclosed; however, Parexel offers competitive entry-level compensation aligned with pharmacovigilance and clinical research industry standards. Professionals can expect: • Structured onboarding and pharmacovigilance training • Exposure to global drug safety operations • Experience working on international regulatory submissions • Strong foundation for long-term careers in patient safety and pharmacovigilance Application Process Eligible candidates can apply directly through the official Parexel careers portal using the link below: Apply Online: https://wd1.myworkdaysite.com/recruiting/parexel/Parexel_External_Careers/job/India—Hyderabad/Patient-Safety-Associate-I_R0000039196 Shortlisted candidates will be contacted by the recruitment team for further steps in the selection process. Frequently Asked Questions Is this role suitable for freshers? Yes. This role is specifically designed for fresh graduates with basic pharmacovigilance knowledge. Is this a permanent position? No. This is a one-year contractual role. Is pharmacovigilance experience mandatory? No. Basic understanding of drug safety concepts is sufficient. Is this an office-based role? Yes. This is a full-time office-based role. Are there growth opportunities after the contract? Yes. High-performing associates may be considered for extended or permanent roles based on business needs. Category Details Company Parexel Vacancies Patient Safety Associate I Required Education MPharm, PharmD, BDS Experience Fresher [...] Read more...

Sitero Mysore Hiring Drug Safety/Sr. Drug Safety Associate

January 19, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Sitero hiring Drug Safety Associate in Mysore. Life Science/Pharma graduates with 1+ year pharmacovigilance experience eligible. Sitero is hiring a Drug Safety Associate (DSA) for its Drug Safety Services team based in Mysore, Karnataka. This role is ideal for life sciences and pharmacy professionals with hands-on experience in pharmacovigilance or clinical research who want to work on end-to-end safety case processing and global regulatory reporting. The position offers exposure to clinical trials and post-marketing safety data within a technology-driven, ethics-focused organization supporting global life sciences clients. Company Overview Sitero is an emerging leader in clinical services and software solutions for the life sciences industry. The organization provides technology-enabled services across early phase studies through Phase III clinical trials, helping sponsors and CRO partners maintain patient safety, regulatory compliance, and operational efficiency. With a strong focus on ethics, innovation, and compliance, Sitero delivers high-touch drug safety and pharmacovigilance services that support regulatory reporting and risk management across global markets. The company’s collaborative culture and emphasis on continuous learning make it a strong workplace for professionals building long-term careers in pharmacovigilance. Job Role & Responsibilities The Drug Safety Associate is responsible for end-to-end pharmacovigilance activities, including safety data review, case processing, and regulatory reporting across clinical and post-marketing environments. Drug Safety Associate (DSA) Key Responsibilities Analyze, review, and interpret safety data from clinical trials, non-clinical studies, literature, and other relevant sources Perform end-to-end case processing of Individual Case Safety Reports (ICSRs) within regulatory timelines Conduct initial evaluation of spontaneously reported adverse events, including post-marketing surveillance reports Identify duplicate and invalid ICSRs and ensure accurate case reconciliation Process safety cases from clinical trials, literature, spontaneous reports, market research, social media, and solicited sources Perform accurate data entry of subject and case information into EDC and safety databases Conduct peer review and quality review of safety cases and EDC data as required Raise and track medical queries to ensure clarity and completeness of safety information Perform accurate medical coding using MedDRA, WHO Drug Dictionary, and company product dictionaries Develop clear, compliant case narratives reflecting appropriate safety information Ensure timely and quality submission of safety cases as per service level agreements Support pharmacovigilance training programs and continuous improvement initiatives Collaborate with Regulatory Affairs teams for timely submission of safety data to health authorities Act as a subject matter expert for vendors supporting drug safety activities Support training and mentoring of Pharmacovigilance Associates These responsibilities directly contribute to patient safety, regulatory compliance, and ethical conduct of clinical research. Eligibility / Qualifications Educational Requirements Degree in Life Sciences, Pharmacy, or equivalent disciplines Relevant Courses (comma-separated): B.Pharmacy, M.Pharmacy, Pharm.D, B.Sc Life Sciences, M.Sc Life Sciences, Clinical Research Experience Requirements Minimum 1+ year of experience in drug safety or clinical research domain Hands-on exposure to pharmacovigilance case processing preferred Preferred Skills & Knowledge Working knowledge of safety databases and coding dictionaries such as MedDRA and WHO-DD Strong understanding of pharmacovigilance regulations and practices Knowledge of US and EU drug safety regulations, CIOMS, and ICH guidelines Experience with safety data from clinical trials, literature, solicited, and post-marketing sources Strong documentation, organizational, and interpersonal skills Ability to collaborate effectively with cross-functional and external stakeholders Excellent verbal and written communication skills Proactive, innovative, and quality-focused mindset Location & Salary Job Location: Mysore, Karnataka Employment Type: Full-time, Permanent Salary: Competitive with variable pay and benefits, aligned with industry standards Compensation & Benefits Competitive fixed and variable pay structure Paid time off Healthcare and retirement benefits Work Schedule & Commitments Standard working hours: 40 hours per week, Monday to Friday Willingness to work in shifts as required Application Process Interested candidates can apply through Sitero’s official hiring channels. Candidates are advised to submit accurate and complete information during the application process. Frequently Asked Questions Who can apply for this Drug Safety Associate role? Candidates with life sciences or pharmacy qualifications and at least 1 year of drug safety or clinical research experience can apply. Is this a clinical trial–only role? No. The role involves safety data from clinical trials, literature, and post-marketing sources. Where is the job located? The position is based in Mysore, Karnataka. Is shift work required? Yes. Willingness to work in shifts is required as per project needs. Is this a permanent role? Yes. This is a full-time, permanent position. Additional SEO Title Options Sitero Hiring Drug Safety Associate – Pharmacovigilance Jobs Mysore Drug Safety & Pharmacovigilance Careers at Sitero Sitero Clinical Research Safety Jobs – Drug Safety Associate Summary Table Company Sitero Vacancies Drug Safety Associate Required Education Life Sciences, Pharmacy Experience Minimum 1+ Year [...] Read more...

Syneos Health Hiring Safety & Pharmacovigilance Specialist I | QC experience

January 9, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Hiring Safety & PV Specialist with life science qualification. 1 vacancy in Gurgaon. Pharmacovigilance, QC, clinical safety role. Syneos Health is hiring a Safety & Pharmacovigilance Specialist I with Quality Control experience for its on-site team in Gurgaon. This role sits at the intersection of clinical research, drug safety, and regulatory compliance, supporting global clinical trials and post-marketing safety activities. If you have hands-on experience in pharmacovigilance case processing and QC review, this position offers exposure to global safety systems, regulated markets, and complex drug development programs. Company Overview Syneos Health is a globally recognized, fully integrated biopharmaceutical solutions organization supporting pharmaceutical, biotechnology, and medical device companies across the entire product lifecycle. With operations spanning more than 110 countries and a workforce of over 29,000 professionals, Syneos Health plays a critical role in clinical development, medical affairs, and commercial execution. The organization has contributed to the development of the majority of novel FDA-approved and EMA-authorized products in recent years. Its operating model places patients and sponsors at the center, combining clinical, safety, and regulatory expertise to accelerate access to safe and effective therapies worldwide. Job Role & Responsibilities As a Safety & PV Specialist I (QC Experience), you will support pharmacovigilance operations across clinical trial and post-marketing programs. The role focuses on Individual Case Safety Report (ICSR) processing, quality control, regulatory compliance, and safety database management. Key responsibilities include: Processing and quality review of ICSRs in accordance with global SOPs, work instructions, and project-specific safety plans Triage and evaluation of safety cases for completeness, accuracy, and regulatory reportability Data entry and maintenance of safety information within validated pharmacovigilance databases Medical coding of adverse events, medical history, concomitant medications, and laboratory tests using MedDRA Preparation of high-quality narrative summaries and identification of follow-up queries Timely submission of expedited safety reports in line with global regulatory timelines Management of duplicate case identification and reconciliation Literature screening and safety surveillance activities Maintenance and validation of xEVMPD product records, including MedDRA coding of indications Execution of activities related to SPOR and IDMP requirements Quality control review of safety cases across clinical trial, spontaneous, and post-marketing sources Filing of safety documents in the Trial Master File (TMF) and Pharmacovigilance System Master File (PSMF) Participation in internal, sponsor, and regulatory audits Continuous application of safety regulatory intelligence to daily PV operations Eligibility / Qualifications Candidates should meet the following criteria: Educational Background Bachelor’s degree in life sciences, pharmacy, nursing, or an equivalent scientific discipline. Equivalent combinations of education and relevant experience may be considered. Relevant courses include: B.Pharm, M.Pharm, B.Sc Life Sciences, M.Sc Life Sciences, Clinical Research, Pharmacology, Nursing, Biotechnology Experience Requirements Minimum 3 years of hands-on experience in pharmacovigilance case processing Demonstrated experience in quality control (QC) review of safety cases Exposure to clinical trial, post-marketing surveillance, and spontaneous adverse event reporting Practical knowledge of safety databases and medical terminology Technical & Professional Skills Strong understanding of ICH GCP, GVP, and global safety regulations Knowledge of clinical trial processes across Phases II–IV Experience with safety reporting timelines and regulatory submissions Proficiency in Microsoft Office tools including Word, Excel, PowerPoint, and Outlook High attention to detail with strong organizational and time management skills Ability to work independently while collaborating effectively within cross-functional teams Clear written and verbal communication skills Location & Salary Job Location: Gurgaon, Haryana (On-site) Employment Type: Full-time Salary: Competitive and aligned with industry standards (commensurate with experience) Application Process Interested candidates can apply online through the official Syneos Health careers portal using the link below: https://syneoshealth.wd12.myworkdayjobs.com/Syneos_Health_External_Site/job/IND-Gurugram/Safety—PV-Specialist-l–QC-Experience-_25104167/apply Frequently Asked Questions (FAQs) Is this role focused on clinical trials or post-marketing safety? The role covers both clinical trial and post-marketing safety, including spontaneous case processing. Is QC experience mandatory for this position? Yes. Prior experience in QC review of pharmacovigilance cases is required. Is this a work-from-home role? No. This position is on-site in Gurgaon. What safety databases are used? Candidates with experience in leading safety databases and MedDRA coding are preferred. Does Syneos Health provide career growth opportunities in PV? Yes. Structured training, internal mobility, and exposure to global programs support long-term career development. Company Syneos Health Vacancies 1 Required Education B.Pharm, M.Pharm, B.Sc/M.Sc Life Sciences, Nursing Experience Minimum 3 years in Pharmacovigilance with QC experience [...] Read more...

Randstand Hiring 30 Drug Safety Trainees – Freshers Pharmacovigilance (₹2.5–4 LPA)

February 11, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Global Pharma Hiring 30 Drug Safety Trainees in Bangalore – Freshers Welcome (₹2.5–4 LPA) A leading global pharmaceutical company, through Randstad, is hiring 30 Drug Safety Trainees for its pharmacovigilance operations in Bangalore (Work From Office). This is a full-time entry-level opportunity open to freshers from Life Sciences and Pharmacy backgrounds, with joining scheduled for March 2026. The role offers structured training in drug safety case processing, adverse event management, medical coding, and global pharmacovigilance standards. The salary range for this position is ₹2.5 to ₹4 LPA, based on qualifications and assessment performance. This opportunity is ideal for candidates who want to build a long-term career in pharmacovigilance, clinical safety, regulatory compliance, and global drug safety operations within a multinational pharmaceutical environment. Company Overview Randstad is a globally recognized talent solutions organization that partners with leading pharmaceutical, biotechnology, and healthcare companies worldwide. Through strategic hiring partnerships, Randstad supports workforce expansion for regulated drug safety and clinical research operations. The hiring organization is a global pharmaceutical company with established pharmacovigilance systems aligned with international regulatory standards including FDA, EMA, ICH, and global safety reporting guidelines. The company operates structured drug safety databases, validated workflows, and compliance-driven case processing systems to ensure patient safety and regulatory adherence. Working in such an environment provides early-career professionals exposure to global safety reporting standards, multinational regulatory frameworks, and structured career progression within the pharmacovigilance domain. Job Role & Responsibilities As a Drug Safety Trainee, you will undergo structured training and gradually handle safety case processing activities under supervision. The role focuses on individual case safety report (ICSR) management and compliance with global pharmacovigilance regulations. ICSR Processing Perform data entry and processing of Individual Case Safety Reports (ICSRs) Review source documents for completeness and accuracy Ensure case processing timelines are met as per global regulatory requirements Adverse Event (AE) & Serious Adverse Event (SAE) Handling Identify and document adverse events from various sources Classify seriousness and expectedness as per safety guidelines Escalate critical cases as required under supervision Medical Coding Perform coding using MedDRA terminology for adverse events Use WHO-DD for product coding and drug dictionary alignment Ensure standardized terminology usage across safety databases PV Documentation & Compliance Maintain accurate pharmacovigilance documentation Support preparation of regulatory safety reports where required Ensure adherence to Good Pharmacovigilance Practices (GVP) Follow internal SOPs and global drug safety standards Learning & Development Participate in training sessions on global safety databases Understand regulatory reporting timelines for FDA, EMA, and other agencies Gain exposure to audit readiness and compliance procedures This role builds strong foundational expertise in global pharmacovigilance operations and prepares candidates for advanced roles such as Drug Safety Associate, PV Specialist, or Safety Reviewer. Eligibility / Qualifications This opportunity is specifically designed for fresh graduates seeking entry into the drug safety domain. Educational Qualifications B.Pharm, M.Pharm, PharmD, B.Sc Life Sciences, M.Sc Life Sciences Relevant disciplines may include: Pharmacology, Pharmaceutical Sciences, Clinical Research, Biotechnology, Microbiology, Biochemistry Experience Requirement Freshers are eligible to apply Basic understanding of pharmacovigilance concepts is an added advantage Required Skills Strong attention to detail Good analytical ability Basic knowledge of medical terminology Good written and verbal communication skills Willingness to work in a structured office environment Location & Salary Job Role: Drug Safety Trainee Location: Bangalore (Work From Office) Joining: March 2026 Open Positions: 30 Salary: ₹2.5 – ₹4 LPA Compensation will be offered based on qualification, assessment results, and company standards. This role provides structured training and strong career growth potential in global pharmacovigilance operations. Application Process Interested and eligible candidates can apply by sending their updated CV to the email below: Email: sahana.s@randstad.in Candidates are advised to mention “Drug Safety Trainee – Bangalore” in the subject line while applying. As there are only 30 openings, early application is strongly recommended. Frequently Asked Questions (FAQs) Who can apply for this Drug Safety Trainee position? Fresh graduates from Pharmacy and Life Sciences backgrounds are eligible. Is prior pharmacovigilance experience required? No. This is a fresher-level opportunity with structured training. What skills will I learn in this role? You will learn ICSR processing, AE/SAE handling, MedDRA coding, PV documentation, and global drug safety compliance. Is this a remote job? No. This is a work-from-office role based in Bangalore. How many vacancies are available? There are 30 open positions. Summary Table Company Global Pharma Company (via Randstad) Vacancies Drug Safety Trainee (30 Positions) Required Education B.Pharm, M.Pharm, PharmD, B.Sc, M.Sc Life Sciences Experience Fresher [...] Read more...

Pharmacovigilance Apprentice Opportunity | Drug Safety Role at Fortrea

February 19, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Fortrea Hiring Apprentice Drug Safety | MSc Life Sciences Freshers | Bangalore Fortrea is hiring an Apprentice – Drug Safety for its Pharmacovigilance department in Bangalore, India. This is a full-time, office-based opportunity designed for fresh postgraduates in Life Sciences who want to build a career in pharmacovigilance, adverse event reporting, clinical trial safety, and global drug safety operations. Candidates with 0–1 year of experience in drug safety or strong exposure to clinical trials during academics are eligible to apply. This entry-level pharmacovigilance role provides structured exposure to safety case processing, SAE/SUSAR reporting, MedDRA coding, periodic safety reports, and regulatory compliance within a global clinical research environment. Company Overview entity is a leading global contract research organization (CRO) providing clinical development, pharmacovigilance, and regulatory services to pharmaceutical, biotechnology, and medical device companies worldwide. The organization supports sponsors across the full clinical development lifecycle, ensuring regulatory compliance, safety surveillance, and data integrity. With a strong global presence, Fortrea works with leading biopharma innovators to accelerate the development of safe and effective therapies. Its pharmacovigilance and drug safety teams play a critical role in adverse event management, signal detection, regulatory reporting, and risk management across multiple therapeutic areas. Job Role & Responsibilities The Apprentice – Drug Safety will support entry-level pharmacovigilance functions in accordance with Fortrea and sponsor Standard Operating Procedures (SOPs). This role focuses on safety data entry, case processing, coding, regulatory reporting support, and compliance documentation. Adverse Event Case Processing Perform data entry of safety data into adverse event tracking systems. Write clear and medically accurate patient narratives. Code adverse events using MedDRA and WHO Drug Dictionary (WHODD) for marketed products where applicable. Assist in listedness assessment against approved product labels. Support causality assessment activities in collaboration with medical staff. Generate queries and collect missing or discrepant information as needed. Regulatory Reporting & Compliance Assist in submission of expedited SAE and SUSAR reports to clients, regulatory authorities, ethics committees, investigators, vendors, and internal stakeholders within defined timelines. Support preparation, review, and approval of Periodic Safety Reports (PSRs) for investigational products and medical devices. Ensure compliance with global pharmacovigilance regulations, GCP guidelines, and safety reporting timelines. Collaboration & Quality Standards Work closely with internal teams and external stakeholders to ensure case completeness and regulatory accuracy. Maintain documentation aligned with sponsor and company quality standards. Participate in departmental activities and support process improvements where required. This position requires strong attention to detail, structured documentation skills, and the ability to manage multiple safety cases within regulatory timelines. Eligibility & Qualifications Educational Qualification Candidates must have completed a Master’s degree in Life Sciences or related disciplines such as: MSc Pharmacology, MSc Biotechnology, MSc Microbiology, MSc Biochemistry, MSc Clinical Research, MSc Life Sciences, MSc Biomedical Sciences, M.Pharm, PharmD. Experience 0–1 year of experience in Drug Safety or Pharmacovigilance. Strong exposure to clinical trials during academic training is preferred. Required Skills Basic understanding of pharmacovigilance regulations and safety reporting processes. Knowledge of MedDRA and WHO Drug Dictionary coding concepts. Strong written and verbal communication skills. Ability to manage multiple tasks and meet strict timelines. Collaborative mindset with ability to work across diverse teams. High level of accuracy and compliance awareness. Fresh postgraduates with strong academic performance and interest in clinical research safety are encouraged to apply. Location & Employment Details Location: Bangalore, India Work Mode: Office-Based Employment Type: Full-Time Experience Level: Entry-Level (Apprentice) Job Requisition ID: 26542 Application Deadline: February 25, 2026 Fortrea offers structured onboarding, exposure to global pharmacovigilance systems, and opportunities for career growth within clinical research and drug safety operations. Application Process Interested candidates can apply directly through Fortrea’s official career portal using the link below: Apply Here: https://fortrea.wd1.myworkdayjobs.com/Fortrea/job/Bangalore/Apprentice-Drug-Safety_26542?source=LinkedIn Applicants should highlight their academic research, clinical trial exposure, safety reporting knowledge, and familiarity with pharmacovigilance concepts in their resume. Career Growth Opportunities With experience, professionals can progress into roles such as: Drug Safety Associate Pharmacovigilance Executive Safety Data Specialist Clinical Safety Scientist Regulatory Safety Officer The pharmacovigilance sector continues to expand globally, driven by increasing regulatory oversight and post-marketing surveillance requirements. Frequently Asked Questions (FAQs) 1. Is this role open to freshers? Yes, fresh postgraduates with 0–1 year of experience are eligible. 2. Is prior pharmacovigilance experience mandatory? No, but strong academic exposure to clinical trials and safety concepts is preferred. 3. What coding dictionaries are used? MedDRA and WHO Drug Dictionary (WHODD) are used for coding adverse events and products. 4. Is this a remote position? No, this is an office-based role in Bangalore. 5. Does the role involve regulatory reporting? Yes, the role includes assisting with expedited safety reports and periodic safety documentation. Summary Table Company Fortrea Vacancies Apprentice – Drug Safety Required Education MSc Life Sciences, MSc Pharmacology, Biotechnology, Microbiology, Biochemistry, M.Pharm, PharmD Experience 0–1 year Drug Safety experience; strong clinical trial exposure preferred [...] Read more...

Fresher Pharmacovigilance Hiring – Elanco Analyst – GDPS (PV Case Processing)

February 18, 2026WhatsApp Group Join Now Telegram Group Join Now Instagram Group Join Now Elanco Hiring Analyst – GDPS (PV Case Processing) | Life Sciences | Bangalore Elanco is hiring for the position of Analyst – GDPS (Global Drug Product Safety) in Bangalore, India. This is a full-time opportunity within the Pharmacovigilance and Drug Safety department, focused on adverse event case processing, regulatory compliance, and safety data management. The role is open to Veterinarians (equivalent to US DVM) with or without pharmacovigilance experience, as well as Life Sciences graduates with 0–2 years of PV experience. If you are looking to build a career in pharmacovigilance, adverse event reporting, regulatory submissions, and global drug safety operations, this role offers structured exposure within a multinational animal health organization. Company Overview entity is a global leader in animal health, dedicated to innovation in preventing and treating diseases in farm animals and companion animals. Listed on the NYSE (ELAN), Elanco operates across international markets with a strong focus on regulatory compliance, product safety, and scientific excellence. The company’s mission centers on improving animal well-being while supporting food safety, sustainability, and veterinary healthcare advancement. With a culture rooted in diversity, collaboration, and continuous learning, Elanco empowers professionals to contribute meaningfully to global pharmacovigilance and product safety systems. Working at Elanco provides exposure to global safety databases, regulatory frameworks, and structured pharmacovigilance processes aligned with international standards. Job Role & Responsibilities The Analyst – GDPS will manage adverse event case processing activities, ensuring data accuracy, regulatory compliance, and timely safety reporting. The role requires precision in documentation, understanding of global PV regulations, and the ability to manage case workflows efficiently. Adverse Event Case Processing Perform data entry of adverse event reports into the pharmacovigilance database. Assess seriousness, causality, and regulatory reportability of adverse event cases. Validate data entries against source documents and call notes. Conduct self-review to ensure case completeness, accuracy, and quality. Determine follow-up requirements for incomplete or unclear cases. Ensure cases are submission-ready for appropriate regulatory authorities. Meet defined productivity and quality benchmarks. Identify potential delays in submission timelines and escalate appropriately. Participate actively in team meetings and contribute to process improvements. Regulatory Compliance & Safety Management Develop understanding of global pharmacovigilance regulations and reporting requirements. Comply with internal SOPs and external regulatory timelines. Support product complaint case processing activities. Maintain adherence to global, local, and regional safety regulations. Manage multiple safety cases across different products simultaneously. The position requires structured thinking, strong documentation skills, and the ability to operate in a compliance-driven environment. Eligibility & Qualifications Educational Background Eligible qualifications include: Veterinarian (equivalent to US DVM degree), B.V.Sc & AH, B.Pharm, M.Pharm, BSc Life Sciences, MSc Life Sciences, Biotechnology, Microbiology, Biochemistry, Pharmacology, or related Life Sciences disciplines. Experience Requirements 0–2 years of pharmacovigilance or drug safety experience for Life Sciences graduates. Veterinarians may apply with or without prior PV experience. Preferred Skills Basic knowledge of medical terminology and adverse event reporting concepts. Understanding of global pharmacovigilance regulations. Strong verbal and written communication skills. Ability to manage multiple products and prioritize workloads effectively. Proficiency in working with multiple databases and Microsoft Office tools. Flexibility to handle high case volumes when required. Self-motivated and adaptable to process changes. Candidates demonstrating strong attention to detail and regulatory awareness will perform well in this role. Location & Employment Details Location: Bangalore, India Employment Type: Full-Time Department: Global Drug Product Safety (GDPS) Job Requisition ID: R0024602 Travel Requirement: 0% Application Process Interested candidates can apply directly through Elanco’s official careers portal using the link below: Apply Here: https://elanco.wd5.myworkdayjobs.com/en-US/External_Career/job/Analyst—GDPS_R0024602?locationCountry=c4f78be1a8f14da0ab49ce1162348a5e Career Growth Opportunities With experience, professionals can advance into roles such as: Senior Pharmacovigilance Associate Drug Safety Specialist Safety Data Management Lead Global Safety Reporting Analyst Pharmacovigilance Quality Reviewer The expanding global animal health and pharmaceutical safety landscape ensures strong career stability in this domain. Frequently Asked Questions (FAQs) 1. Is this role open to freshers? Yes, Life Sciences graduates with 0–2 years of experience are eligible. 2. Are veterinarians eligible? Yes, veterinarians (equivalent to US DVM) can apply with or without prior PV experience. 3. Is prior pharmacovigilance experience mandatory? It is preferred but not mandatory for eligible candidates. 4. What type of cases will be handled? The role involves adverse event case processing and product complaint case management. 5. Is this a remote position? No, this is an on-site role based in Bangalore. Summary Table Company Elanco Vacancies Analyst – GDPS (PV Case Processing) Required Education DVM, B.V.Sc & AH, B.Pharm, M.Pharm, BSc/MSc Life Sciences, Biotechnology, Microbiology, Biochemistry Experience 0–2 years pharmacovigilance experience; veterinarians may apply with or without PV experience [...] Read more...

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