Role & responsibilities 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
Preferred candidate profile
Basic knowledge of MS Office (Word, Excel, PowerPoint)
Positive written and verbal communication skills
Attention to detail and documentation discipline
Willingness to learn and work in a regulated, compliance-driven environment
📌 Pharmacovigilance Associate (Chennai)
🏢 Airvin Skills
📍 Chennai
Reply to this offer
Impress this employer describing Your skills and abilities, fill out the form below and leave Your personal touch in the presentation letter.