Drug Safety Associate

Role & responsibilities

A Drug Safety Associate to support drug safety operations by processing adverse event cases and

ensuring compliance with global pharmacovigilance regulations.

Key Responsibilities

Receive, triage and process adverse event/drug safety reports

Perform case data entry, narrative writing and quality review

Coordinate with pharmacovigilance physicians for case assessment

Track case processing timelines to meet regulatory reporting deadlines

Support preparation of aggregate/periodic safety reports

Maintain drug safety databases with accuracy and compliance

Stay updated on GVP and other pharmacovigilance regulatory requirements

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