Jobs at Nurix Therapeutics

Develop, optimize, and validate antibody bioconjugation chemistries scalable from bench to multi-mg production. Design automation-ready protocols, execute conjugation runs, purify and characterize conjugates (FPLC, TFF, HPLC, LC-MS), write SOPs and technical reports, train automation staff, and collaborate cross-functionally with chemistry, protein biochemistry, computational teams, and CROs/CDMOs.

Lead end-to-end IT infrastructure and operations including cybersecurity operations, end-user services, and ITSM. Consolidate MSPs, build a SOC, align research and scientific computing with IT, manage AWS/HPC/container environments, establish IAM, and improve vendor and service management.

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

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.

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

Lead global value, pricing, and access strategy and co-lead the US launch for a hematology product. Design payer engagement, pricing and contracting, patient support, and trade/channel plans. Partner with a global pharma collaborator and internal teams (HEOR, Medical Affairs, Marketing, Sales) to build evidence, economic models, and launch readiness while advising senior leadership and the Board.

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 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.