We are looking for a detail-oriented Pharmacovigilance Associate to join our Drug Safety team. The candidate will be responsible for processing and reviewing Individual Case Safety Reports (ICSRs), ensuring accurate documentation and supporting pharmacovigilance activities in compliance with regulatory guidelines.

Roles and Responsibilities

- Collect, review and process Individual Case Safety Reports (ICSRs).
- Perform data entry and case processing in pharmacovigilance databases.
- Identify and assess Adverse Events (AEs) and Responsible Adverse Events (SAEs).
- Perform medical coding using MedDRA and WHO Drug dictionaries.
- Conduct case narrative writing and quality checks.
- Follow up on missing information related to safety cases.
- Ensure compliance with applicable pharmacovigilance regulations and SOPs.
- Meet quality and productivity targets within defined timelines.

Contact HR - Subashree: (phone hidden)

Educational Qualification

B.Pharm / M.Pharm / Pharm.D / B.Sc / M.Sc (Life Sciences) or equivalent relevant qualification.

📌 Pharmacovigilance Associate (Bengaluru)
🏢 Reqras Research
📍 Bengaluru