Jobs at Nurix Therapeutics

Support in vitro and in vivo ADME/DMPK studies by developing and qualifying bioanalytical LC-MS/MS methods, quantitating small molecules, metabolites and biomarkers, performing MetID and stability assays, operating and troubleshooting LC-MS/MS systems, managing CRO bioanalytical projects, maintaining electronic lab notebooks, and collaborating cross-functionally to deliver PK/PD and non-GLP study support.

Lead development and execution of global regulatory strategy for oncology (solid tumors), manage preparation of high-quality IND/CTA/NDA/MAA submissions, interact with health authorities, track submission deliverables, and guide cross-functional teams to mitigate regulatory risk and ensure compliance.

Lead and own clinical data management strategy, deliverables, and teams across multiple oncology studies. Ensure CDISC/CDASH/GCDMP compliance, manage vendors, design eCRFs/EDC, maintain inspection readiness, oversee data cleaning/reconciliation, and partner with clinical, biometrics, and senior stakeholders to support regulatory submissions and study reporting.

Coordinate and schedule interviews, manage candidate communications and logistics, maintain records in Greenhouse, support recruiters and hiring managers, arrange travel and onsite visits, monitor recruiting activity for accuracy and compliance, and assist with TA projects, reporting, and employer branding to deliver an excellent candidate experience.

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.

Lead full-cycle recruiting for scientific, technical, and corporate roles at a biotech company. Partner with hiring managers to define needs, source passive candidates, manage interviews, offers, and ATS data in Greenhouse, and improve recruiting processes and employer brand.

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.

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.

Lead Nurix's nonclinical safety function, set toxicology and safety pharmacology strategy across discovery through clinical development, manage internal team and CRO relationships, oversee IND-enabling GLP/non-GLP studies and regulatory submissions, advise senior leadership and external stakeholders, and represent toxicology in business development and regulatory interactions.

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

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.