Cencora hiring Trainee Specialist Pharmacovigilance
- Cencora hiring Trainee Specialist Pharmacovigilance in Noida. B Pharma, M Pharma, Life Science graduates eligible. Full-time vacancy.
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities
- Eligibility / Qualifications
- Required Education
- Skills & Competencies
- Location & Employment Details
- Application Process
- Frequently Asked Questions (FAQs)
- Is this position suitable for freshers?
- What qualifications are eligible for this role?
- Is prior pharmacovigilance experience mandatory?
- What are the career growth opportunities?
- Is this a full-time role?
- Equal Employment Opportunity Statement
- Job Summary Table
Cencora hiring Trainee Specialist Pharmacovigilance in Noida. B Pharma, M Pharma, Life Science graduates eligible. Full-time vacancy.
Cencora is hiring for the position of Trainee – Specialist, Pharmacovigilance, Epidemiology & Risk Management at its Noida location. This opportunity is designed for pharmacy and life sciences graduates who want to build a long-term career in drug safety, regulatory compliance, and risk management within the global pharmaceutical and healthcare consulting ecosystem. The role offers hands-on exposure to real-world pharmacovigilance operations, international regulatory standards, and safety data management practices that directly impact patient safety and public health.
Company Overview
Cencora is a global healthcare services organization committed to improving access to medicines and advancing patient care worldwide. With a strong presence across pharmaceutical distribution, regulatory consulting, pharmacovigilance, and healthcare analytics, Cencora supports pharmaceutical, biotechnology, and life sciences companies throughout the product lifecycle. The organization emphasizes ethical practices, regulatory compliance, and innovation in healthcare delivery.
At Cencora, employees are not just resources but contributors to a shared mission of creating healthier futures. The company operates with high standards of governance, quality, and compliance, making it a trusted partner for global pharmaceutical companies and regulatory authorities. In India, Cencora operates through its affiliated entity PharmaLex India Private Limited, delivering specialized consulting services in pharmacovigilance, regulatory affairs, and epidemiology.
Job Role & Responsibilities
As a Trainee – Specialist in Pharmacovigilance, Epidemiology & Risk Management, you will be responsible for supporting core drug safety operations under global regulatory frameworks. This role focuses on Individual Case Safety Report (ICSR) processing, adverse event management, and regulatory reporting, ensuring patient safety and compliance with international guidelines.
Key Responsibilities
- Perform triage and initial validity assessments of adverse event cases received from spontaneous reports, clinical trials, literature sources, and health authority communications
- Conduct accurate and timely data entry into pharmacovigilance and drug safety databases
- Complete initial ICSR assessments in line with regulatory requirements and internal quality standards
- Evaluate cases for seriousness, expectedness, and causality to determine expedited reporting obligations
- Ensure compliance with global reporting timelines to Health Authorities and client partners
- Prepare standardized regulatory reporting documents such as CIOMS I forms, MedWatch forms, and XML submissions
- Initiate and manage follow-up requests to collect missing or additional safety information
- Maintain thorough and audit-ready case documentation throughout the case lifecycle
- Perform ICSR searches and retrieval from the EVWEB database, including company and non-company case assessments
- Support operational tasks and additional assignments as directed by the supervisor
This role provides deep exposure to pharmacovigilance case processing, regulatory compliance, and global drug safety standards, making it ideal for candidates aiming to grow into pharmacovigilance analyst, drug safety associate, or regulatory specialist roles.
Eligibility / Qualifications
Required Education
Candidates must have completed one of the following qualifications:
B Pharma, M Pharma, BDS, BSc Life Sciences, MSc Life Sciences, Clinical Research, Biotechnology, Microbiology, Biochemistry
Fresh graduates and early-career professionals with an interest in pharmacovigilance, epidemiology, and risk management are encouraged to apply.
Skills & Competencies
- Strong written and verbal communication skills
- High attention to detail and accuracy in data handling
- Ability to work under strict regulatory timelines
- Basic understanding of pharmacovigilance processes and drug safety reporting standards is preferred
- Willingness to learn global regulatory requirements such as ICH, FDA, EMA, and WHO guidelines
Location & Employment Details
- Location: Noida, Uttar Pradesh, India
- Employment Type: Full-time
- Department: Consulting – Pharmacovigilance and Risk Management
- Posted Date: January 5, 2026
Salary details are not disclosed and will be aligned with industry standards, candidate qualifications, and internal compensation structures.
Application Process
Interested candidates can apply directly through the official Cencora careers portal using the link below:
Ensure your resume highlights relevant education, pharmacovigilance knowledge, internships, or certifications related to drug safety, clinical research, or regulatory affairs.
Frequently Asked Questions (FAQs)
Is this position suitable for freshers?
Yes. This role is suitable for fresh graduates from pharmacy and life sciences backgrounds who want to start a career in pharmacovigilance and drug safety.
What qualifications are eligible for this role?
B Pharma, M Pharma, BDS, and Life Science graduates such as BSc or MSc in Biotechnology, Microbiology, Biochemistry, or related fields are eligible.
Is prior pharmacovigilance experience mandatory?
No. Prior experience is not mandatory. However, basic knowledge of pharmacovigilance concepts is preferred.
What are the career growth opportunities?
Candidates can progress to roles such as Drug Safety Associate, Pharmacovigilance Analyst, Senior PV Specialist, or Regulatory Safety Consultant.
Is this a full-time role?
Yes. This is a full-time position based in Noida.
Equal Employment Opportunity Statement
Cencora is an equal opportunity employer and does not discriminate based on race, gender, age, religion, disability, or any other protected category. The organization is committed to maintaining a fair, inclusive, and respectful workplace.
Job Summary Table
| Company | Cencora (PharmaLex India Private Limited) |
|---|---|
| Vacancies | Trainee – Specialist, Pharmacovigilance, Epidemiology & Risk Management |
| Required Education | B Pharma, M Pharma, BDS, BSc Life Sciences, MSc Life Sciences |
| Experience | Freshers / Entry-Level |
To apply for this job please visit careers.cencora.com.
