Nurix Therapeutics
Senior Manager/Associate Director, Regulatory Affairs (Strategy, Hematology Oncology)
Brisbane, California, United States · Director
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odds of building a lasting career here
Sponsors, but it's cap-subject — you still face the weighted lottery (~61% per draw at Level IV). Good if you win; have a cap-exempt backup on your list.
Lottery odds assume a STEM candidate.
Personalize to your clock →H-1B wage level
the lottery is wage-weighted — each level is one more entry
Level III starts at $211,328 — $23,528 above the bottom of this range, and above its posted ceiling.
DOL prevailing wage, 2026-27 wage year · Managers, All Other (11-9199) · San Francisco-Oakland-Fremont, CA. Wage level is derived by USCIS from the offered wage, occupation and worksite; the occupation shown is inferred from the job title.
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About the role
- In this role, you will be a core member of the Regulatory team and will be responsible for helping build and execute on global regulatory strategy, objectives, policies and programs pertaining to development and future marketing of products.
Responsibilities
- Provides regulatory strategic direction and support for assigned global development programs/development program activities
- Designs and implements regulatory strategies with Regulatory Affairs staff to obtain and maintain product investigative and marketing applications for assigned programs, as well as their life cycle management
- Collaborate with cross-functional teams to ensure product compliance throughout the development lifecycle
- Monitor and assess regulatory risks and develop mitigation strategies
- Plays an essential part in defining requirements for, implementing, and supporting future systems and tools to be employed by Nurix in the areas of document management, submission content planning, and regulatory information management
- Tracks the status of major deliverables for regulatory submissions (e.g., study reports, summary documents, labeling) along with their dependencies
- Develops and maintains submission plan templates to ensure Nurix regulatory submissions are consistently planned and executed across programs
- Manages consultants and contractors as needed
Nice to have
- Bachelor's degree in life-sciences or related scientific discipline
- advanced degree preferred Manager:
Skills
- Bachelor's degree in life-sciences or related scientific discipline; advanced degree preferred
- Must have minimum of 8 years in Regulatory affairs strategy
- Strong demonstration of knowledge of drug development, FDA, EMA and ICH guidelines and regulations
- Ability to read, analyze and interpret scientific and technical information, as well as regulatory
- Ability to comply with changing regulatory
- Strong project management and critical thinking skills
- Excellent organizational and communication skills, both written and verbal
- Positive attitude, energetic and proactive
- Bachelor's degree in life-sciences or related scientific discipline; advanced degree preferred Manager:
- Strong interpersonal skills and the ability to effectively work with others
- Fit with Nurix Culture and Values
- Strong team orientation; highly collaborative
Compensation
- SM $187,800 - $208,638 AD $199,500 - $231,200
- Assist in the preparation and maintenance of Annual Reports, Development Safety Update Reports (DSURs), Investigator's Brochures and other documents required for INDs, CTAs, NDAs and other related regulatory development and marketing applications
Benefits
- Experience providing hands-on support for planning clinical trial and marketing applications to health authorities including but not limited to FDA, EMA
This listing is sourced directly from Nurix Therapeutics's careers page and normalized into a canonical job model.