Partnering with a clinical-stage biotech building in oncology as they look for a Senior Manager, Pharmacovigilance to take ownership of end-to-end PV activities across global clinical programs. This is an opportunity to blend hands-on execution with strategic oversight.
You’d be stepping into a highly visible role, working cross-functionally to drive safety strategy, oversee vendors, and support regulatory deliverables across development.
This role is onsite, based in San Diego and ideal for someone who enjoys being close to the science and the team.
What you’ll bring:
• 8+ years in pharmacovigilance (biotech/pharma experience required)
• Strong knowledge of global PV regulations (FDA, EMA, ICH)
• Experience in safety surveillance, signal detection, and aggregate reporting
• Background in oncology (additional autoimmune a plus)
• Proven vendor oversight + cross-functional collaboration