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 setting

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