Accenture Fresher Pharmacovigilance Vacancies – PV Services Associate in Chennai
- Accenture Hiring Pharmacovigilance Services Associate – Drug Safety & ICSR Processing | 0–2 Years | Bengaluru
- Company Overview
- Job Role & Responsibilities
- Core Responsibilities
- Eligibility / Qualifications
- Educational Qualification
- Experience
- Required Skills
- Location & Employment Details
- Why This Role Is Important in Drug Safety
- Application Process
- Frequently Asked Questions (FAQs)
- 1. Who can apply for this Pharmacovigilance role at Accenture?
- 2. Is this role suitable for freshers?
- 3. What databases or tools should candidates know?
- 4. What types of cases will be handled?
- 5. What career growth opportunities are available?
- Recruitment Summary
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:
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 |
To apply for this job please visit www.accenture.com.
