An entry-level Pharmacovigilance Associate to support drug safety monitoring activities, including
adverse event case processing and safety database management.
Key Responsibilities
- Process Individual Case Safety Reports (ICSRs) for adverse events
- Perform MedDRA coding of adverse event and medical history terms
- Enter and review safety data in pharmacovigilance/drug safety databases
- Support signal detection and safety data analysis activities
- Assist in preparing periodic safety reports (PSUR/PBRER)
- Ensure compliance with GVP (Good Pharmacovigilance Practices) guidelines
- Support literature screening for safety-relevant information
Educational Qualification
B. Pharm/M. Pharm, B. Sc/M. Sc Life Sciences, MBBS, BDS, or PG Diploma in Pharmacovigilance.
Experience Required
Fresher / 0-1 year. Freshers with the right educational background and a willingness to learn are
strongly encouraged to apply. On-the-job training will be provided.
Good to Have
- Basic knowledge of MS Office (Word, Excel, Power Point)
- Valuable written and verbal communication skills
- Attention to detail and documentation discipline
- Willingness to learn and work in a regulated, compliance-driven environment
📌 Pharmacovigilance Associate (Bengaluru)
🏢 LLRI - Learning Labb Research Institute
📍 Bengaluru
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