Description
The role supports ICSR management and pharmacovigilance activities for a client and company, including processing Individual Case Safety Reports, following up on reports, managing SAE/SUSARs, reconciling clinical and partner data, handling product quality complaints, and coding using MedDRA and WHO. It may also support the RA and PV Network Department and act as a local pharmacovigilance contact or local screening responsible person. The position requires a life-science, pharmacy, nursing, or healthcare-related qualification or experience, 0–1 year of pharmacovigilance experience, strong organization and management skills, advanced English, and advanced Microsoft Office literacy.
