Indegene is hiring experienced professionals for the position of Drug Safety Associate through a Walk-in Interview on 29 August 2026 in Bengaluru. The role is focused on Pharmacovigilance (PV), Individual Case Safety Report (ICSR) processing, case quality review, adverse-event identification, MedDRA/product coding, narrative writing and end-to-end case processing. Candidates with 2–5 years of relevant PV/ICSR experience, hands-on knowledge of the Argus Safety Database, and strong understanding of ICH & GVP guidelines are encouraged to attend.
💊 Job Details
Position: Drug Safety Associate
Experience: 2–5 years of PV/ICSR experience
Location: Bengaluru
Work Mode: Work from office — Bangalore only; no remote option
📋 Key Responsibilities
- Process individual case safety reports (ICSRs) accurately and in compliance with requirements.
- Identify serious adverse events and special scenarios.
- Perform duplicate searches.
- Conduct coding using MedDRA and product dictionaries.
- Perform narrative writing.
- Conduct quality reviews and follow-ups.
- Ensure adherence to SOPs and data-integrity requirements.
- Handle end-to-end case processing and quality activities.
🎓 Must-Have Requirements
- Qualified healthcare professional.
- Minimum 2–5 years of PV/ICSR experience.
- Hands-on experience with Argus Safety Database.
- Strong knowledge of ICH & GVP guidelines.
- Freshers and candidates with less than 2 years of PV experience are not eligible.
- Candidates should preferably have a 30–60 day notice period.
- Career gaps exceeding 6 months are not considered.
- Currently, candidates based in Bangalore only are being considered.
📅 Walk-in Interview Details
- Date: 29 August 2026
- Time: 10:00 AM – 1:00 PM
- Venue: Aspen G-4 Block, Manyata Tech Park, Bengaluru
- Contact Person: Augustine Raj
🎯 Ideal Candidate Profile
This opportunity is best suited for professionals already working in Pharmacovigilance, Drug Safety, ICSR Case Processing or Clinical Safety, particularly those with practical experience in Argus, MedDRA coding, case narratives, duplicate searches, serious-event assessment, quality review and regulatory compliance.
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