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 …