Dendreon is looking for a Senior Medical Director (Pharmacovigilance) with 5+ years pharmaceutical/safety experience and PV management experience. This position ensures that safety practices are supported globally.
This position is responsible for managing all of the PV operations/activities associated with collecting, processing, and reporting spontaneous adverse drug reactions for Dendreon’s marketed products, and serious adverse events from clinical trials. This position also serves as a lead on global committees and task forces to ensure the alignment of safety processes across the sites are in compliance with appropriate regulations.
The director interacts with senior leaders of other functions including clinical, regulatory, data management and quality, as well as external vendors. This person works independently with limited supervision, and makes decisions based on a thorough understanding of Dendreon’s products and processes.
Minimal travel <10%.