Job DescriptionRole Overview

NAn entry-level Pharmacovigilance Associate to support drug safety monitoring activities, including

Nadverse event case processing and safety database management.

NKey Responsibilities

n■ Process Individual Case Safety Reports (ICSRs) for adverse events

N■ Perform MedDRA coding of adverse event and medical history terms

N■ Enter and review safetydata in pharmacovigilance/drug safety databases

N■ Support signal detection and safety data analysis activities

N■ Assist in preparing periodic safety reports (PSUR/PBRER)

N■ Ensure compliance with GVP (Good Pharmacovigilance Practices) guidelines

N■ Support literature screening for safety-relevant information

NEducational Qualification

NB.Pharm/M.Pharm,



B.Sc/M.Sc Life Sciences, MBBS, BDS, or PG Diploma in Pharmacovigilance.

NExperience Required

nFresher / 0-1 year. Freshers with the right educational background and a willingness to learn are

Nstrongly encouraged to apply. On-the-job training will be provided.

NGood to Have

n■ Basic knowledge of MS Office (Word, Excel, PowerPoint)

N■ Good written and verbalcommunication skills

N■ Attention to detail anddocumentation discipline

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

📌 Hiring: Pharmacovigilance Associate (Karnataka)
🏢 LLRI - Learning Labb Research Institute
📍 Karnataka