Pharmacovigilance Team Member

This role involves end-to-end processing of adverse event reports, ensuring accurate data entry, quality checks, and timely reporting to regulatory authorities in compliance with legislative requirements. The position requires analyzing scientific texts, applying pharmacovigilance regulations, and collaborating with internal teams and external stakeholders to maintain patient safety standards. Candidates will manage case intake, perform MedDRA coding, and conduct monthly reconciliations while adhering to strict deadlines.