Job Title

Position Summary 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 AIintegrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurixs dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degraderbased treatments at the forefront of patient care, writing medicines next chapter with a new script to outmatch disease. This role owns the business systems that support Nurix''s path from clinical trials through commercialization. You will be the primary IT partner to Clinical Operations, Regulatory, Quality, and Commercial leadership, ensuring the technology they depend on works and evolves with the business. Primary Responsibilities Serve as primary IT partner to Clinical Operations, Regulatory, Quality, and Commercial Translate business needs into system requirements and implementation plans Own stakeholder satisfaction for the enterprise applications portfolio Proactively identify technology opportunities that enable business outcomes Application Portfolio Management Own the clinical, quality, regulatory, and commercial application portfolio Current systems: Medidata Rave (EDC), Wingspan eTMF, Argus (pharmacovigilance), Veeva Vault RIM (submissions), Veeva CRM, Veeva QMS, VeevaDocs, Veeva Training ERP/backoffice systems as commercial operations expand Define application roadmap aligned to clinical milestones and commercial readiness Manage system integrations, data flows, and reporting needs Implementation and Delivery Lead implementations endtoend: requirements, configuration, testing, training, golive Coordinate with clinical PM contractor on project execution Align with IT Project Manager on resource conflicts, shared vendors, and portfolio reporting Manage UAT coordination, training development, and change management Vendor Management Own functional relationships with application vendors (what gets built, does it work, is it adopted) Partner with Director, IT Strategy & Vendor Operations on contracts, SOWs, and vendor governance Hold vendors accountable for delivery outcomes and service quality Ensure vendors build internal capability, not dependency Compliance and Quality Partner with Quality on GxP validation requirements for regulated systems Understand CSV principles; work alongside Qualitas and internal validation resources Support FDA inspection readiness for ITrelated controls Ensure 21 CFR Part 11 compliance for electronic records and signatures organization Required Qualifications 10+ years in IT, with 5+ years in life sciences or pharmaceutical environments Direct experience with clinical systems: EDC, eTMF, CTMS, safety/PV, or regulatory submissions Veeva platform experience (Vault, CRM, QMS) Medidata Rave experience Track record leading application implementations from requirements through adoption Experience managing vendors for delivery outcomes (not just contract administration) Working knowledge of GxP validation principles and 21 CFR Part 11 Strong business analyst skills: requirements gathering, process design, stakeholder facilitation Comfortable with handson configuration and troubleshooting when needed Effective communicator with scientific, clinical, and business audiences Bachelor''s degree in a technical field, or equivalent experience Strongly Preferred Qualifications Experience supporting regulatory submissions or FDA inspection readiness Commercial systems experience (CRM, market access, patient services) ERP implementation or administration experience Organization Reports to: SVP IT Key Partners Director, IT Operations (contracts, vendor governance, shared infrastructure) IT Project Manager (portfolio coordination, resource alignment) Clinical PM contractor (implementation project execution) Sr. Director and CISO (security, compliance) USDM (system validation, GxP compliance) Primary Stakeholders Clinical Operations leadership Regulatory Affairs leadership Quality leadership Commercial leadership Salary Range $216,000 to $251,000 Plus Bonus and Equity Location Brisbane, CA - Onsite Nurix Therapeutics, Inc. is committed to protecting and respecting your privacy and personal information, including information collected by Nurix when you apply for a job with Nurix or in the course of your employment with Nurix. By applying for a position at Nurix, you agree to our collection and use of personal information as described in our Privacy Policy (#J-18808-Ljbffr