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 safety data 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■ Valuable written and verbal communication skills
n■ Attention to detail and documentation discipline
n■ Willingness to learn and work in a regulated, compliance-driven environment

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