Role Overview An 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 Med DRA 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 arestrongly encouraged to apply. On-the-job training will be provided. Good to Have■ Basic knowledge of MS Office (Word, Excel, Power Point)■ Good written and verbal communication skills■ Attention to detail and documentation discipline■ Willingness to learn and work in a regulated, compliance-driven setting

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