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About the role
• Serve as the PVO Lead for assigned products, representing PV operations in cross-functional clinical team meetings. • Support SAE reconciliation activities in partnership with Clinical Operations and Data Management.
What they're looking for
- Education & Experience
- • Bachelor's degree in Life Sciences, Pharmacy, Nursing, or a related field required, advanced degree (PharmD, MS, PhD) preferred
- • Minimum of 8–10 years of pharmacovigilance/drug safety experience, including significant experience in PV operations, ICSR management, and clinical safety support
- • Prior experience managing or overseeing PV vendors/CROs required
- • Experience with managing PV budget and invoicing
- • Experience supporting regulatory inspections and audits (FDA, EMA, or other health authorities) strongly preferred
More about this role
Associate Director, Pharmacovigilance Operations
Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix’s dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine’s next chapter with a new script to outmatch disease.
The Associate Director, Pharmacovigilance Operations (PVO) is responsible for all PV operational and compliance aspects of assigned Nurix products across the product lifecycle — from First-In-Human (FIH) studies through post-marketing — and for oversight of the end-to-end management of Individual Case Safety Reports (ICSRs).
This role serves as the PVO lead for assigned products, driving in-stream quality...
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