Pharmacovigilance Associate

Role OverviewAn entry-level Pharmacovigilance Associate to support drug safety monitoring activities, includingadverse 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 (Good Pharmacovigilance Practices) guidelines■ Support literature screening for safety-relevant informationEducational QualificationB.Pharm/M.Pharm, B.Sc/M.Sc Life Sciences, MBBS, BDS, or PG Diploma in Pharmacovigilance.Experience RequiredFresher / 0-1 year. Freshers with the right educational background and a willingness to learn arestrongly 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