The Senior Director, Safety and Pharmacovigilance (PV) will lead and manage global PV activities across clinical programs, ensuring regulatory compliance and high-quality safety reporting.
Responsibilities include overseeing adverse event processing, aggregate reporting, safety document preparation, medical review collaboration, vendor management, process improvements, and participation in inspections and audits.
Requirements include 5+ years in Drug Safety/PV within biopharma/biotech, healthcare professional background, knowledge of global PV regulations, safety databases, and strong project management skills.
We value a passionate, innovative, and inclusive team environment, offering comprehensive benefits, a collaborative culture, and competitive salary ($265,000 - $280,000).