Role Overview An entry-level Pharmacovigilance Associate to support drug safety monitoring activities, including adverse 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 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 are strongly encouraged to apply. On-the-job training will be provided. Good to Have ■ Basic knowledge of MS Office (Word, Excel, PowerPoint) ■ Valuable written and verbal communication skills ■ Attention to detail and documentation discipline ■ Willingness to learn and work in a regulated, compliance-driven environment

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