Pharmacovigilance Associate

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)

Good written and verbal communication skills

Attention to detail and documentation discipline

Willingness to learn and work in a regulated, compliance-driven environment