Teams at Nurix Therapeutics

Leads global clinical development programs from Phase 1 through approval and launch. Provides medical oversight for clinical trials, protocol design, safety and clinical data review, regulatory interactions, CRO and operational oversight, and cross-functional program leadership. Partners with executive, scientific, regulatory, commercial, and technical teams to develop strategy, manage risks, support IND/NDA/MAA activities, and communicate program results to internal and external stakeholders.

The Associate Director will manage the Computer Systems Assurance program, ensuring compliance with regulatory guidelines, leading validation activities, and supporting operational quality within a biotech environment.

Perform bioanalytical method development and LC-MS/MS quantitation for in vitro and in vivo ADME/DMPK studies, including MetID with LC-QTOF, PK sample analysis, CRO project management, data reporting, and maintaining electronic lab notebooks to support drug discovery programs.