Jobs at Nurix Therapeutics

The Senior Clinical Trial Manager oversees global clinical trial operations, vendor management, regulatory compliance, and team leadership to ensure successful trial implementation from start to finish.

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.

The Scientist will lead analytical method development, characterize materials, oversee external manufacturing partners, and ensure compliance with quality standards, contributing to drug development at Nurix Therapeutics.

Lead global and US marketing strategy for Nurix Therapeutics, driving brand development, launch readiness, commercial strategy, market insights, forecasting, field engagement, agency/vendor partnerships, and lifecycle planning to support commercialization of hematology/oncology assets.

The Associate Director of Regulatory Affairs in Hematology Oncology will develop and execute regulatory strategies, ensure compliance in submissions, and support clinical development across teams.

The Protein Expression Research Associate will coordinate and execute activities necessary for recombinant protein expression in insect and mammalian cell systems, document results, and maintain cultures.

The Director of Regulatory Affairs develops global regulatory strategies and leads interactions with health authorities for clinical submissions, focusing on immunology and inflammation.

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.

The Sr. Biosample Manager will oversee the lifecycle management of clinical biosamples, ensuring compliance and collaboration with internal and external stakeholders to support translational research.

The Senior Manager, Quality Operations ensures GMP compliance in clinical development, manages quality systems, oversees manufacturing operations, conducts audits, and supports inspections.

The Senior Associate will support regulatory submissions, ensure compliance, manage documentation processes in Veeva RIMS, and assist in preparation and review of regulatory documents for health authorities.

The Manager leads analytical CMC activities, ensuring method transfer, data interpretation, and alignment across teams. They manage regulatory submissions and oversee partnerships.