Senior Pharmacovigilance Associate

This role involves managing Individual Case Safety Reports (ICSRs) and supporting Pharmacovigilance (PV) processes in strict compliance with regulations and client requirements. Key duties include SAE/SUSAR management, data reconciliation, medical coding using MedDRA and WHO standards, and handling product quality complaints. The position also requires acting as the Local Contact Person for Pharmacovigilance and fostering collaboration across the PV network.