Pharmacovigilance Associate

Full-time other-general

Role Summary

The Pharmacovigilance Associate is responsible for supporting drug safety operations through the review, processing, and assessment of adverse event reports. This role ensures accurate data handling, timely case processing, and compliance with global pharmacovigilance standards while contributing to patient safety and regulatory obligations.

Key Responsibilities

• Review and process adverse event and product safety reports within required timelines
• Perform accurate case data entry, coding, and duplicate checks in safety databases
• Draft concise and medically accurate case narratives and follow-up queries
• Conduct initial case assessments based on established procedures and guidelines
• Maintain documentation, trackers, and quality records related to case processing
• Ensure compliance with internal SOPs, quality standards, and regulatory requirements
• Collaborate w...