Role Overview

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 (Positive 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, PowerPoint)

■ Good written and verbal communication skills

■ Attention to detail and documentation discipline

■ Willingness to learn and work in a regulated, compliance-driven environment

📌 Pharmacovigilance Associate (Yelahanka)
🏢 LLRI - Learning Labb Research Institute
📍 Yelahanka