Nurix Therapeutics
Director / Sr. Director, Regulatory Affairs (Strategy, Oncology Solid Tumors)
Brisbane, California · Director
Stay score
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
$19,014 more — $251,014 — moves this role to Level IV and 4 lottery entries. That figure is inside the range the employer already advertised.
Based on the DOL prevailing wage for this occupation and worksite, a base salary of $251,014 would place this position at wage Level IV. That figure is within the posted range, and I'd like to target it. This role classifies under "Managers, All Other" for prevailing-wage purposes.
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.
Employer immigration record
from this employer's Department of Labor filings
Files H-1B transfers
Sourced from Department of Labor LCA, PERM and prevailing-wage disclosure data. Employer matching is by name, so figures may be split across an employer's legal entities. Absence of a filing means none appears in our copy of the data, not that none exists.
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About the role
- Nurix Therapeutics, Inc. is seeking a Director/ Sr.
- Director, Regulatory Affairs (Strategy, Oncology - Solid Tumors) to join the Regulatory team.
- The successful candidate will be a core member of the Regulatory team working in close collaboration with the SVP, Head of Regulatory Affairs and other cross-functional colleagues.
Responsibilities
- Develop a comprehensive regulatory strategy that takes into account worldwide regulatory requirements to drive product development, global registration, achievement and maintenance of desired regional labeling, and effective regulatory agency interactions
- Lead and manage the development and preparation of high-quality global submissions (including IND, CTAs, NDAs, and MAAs) for early and late-stage programs in collaboration with the regulatory and project teams to support and accelerate clinical development and regulatory approval, as applicable
- Develops and executes, or oversees global regulatory strategy for long-term planning, including the potential to accommodate expedited development needs
- 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
- Manage consultants and contractors as needed
- Proven ability to manage multiple projects, identify and resolve regulatory issues
Requirements
- It also ensures adherence to relevant regulatory requirements and company Standard Operating Procedures (SOPs) as required.
Nice to have
- Bachelor's degree in life-sciences or related scientific discipline
- advanced degree preferred
Skills
- Bachelor's degree in life-sciences or related scientific discipline; advanced degree preferred
- Must have minimum of 12 years in Regulatory affairs strategy with significant experience in the oncology (solid tumors) therapeutic area
- Strong demonstration of knowledge of drug development, FDA, EMA and ICH guidelines and regulations
- Strong project management and critical thinking skills
- Excellent organizational and communication skills, both written and verbal
- Positive attitude, energetic and proactive
- Strong interpersonal skills and the ability to effectively work with others
- Strong team orientation; highly collaborative
- Solutions and results-oriented focus
- Nurix Culture and Values
- Hands-on approach; resourceful and open to diverse points of view
Compensation
- Salary Range: Director: $232K - $274K
Benefits
- Support communication with global Health Authorities (HA), such as FDA and EMA, including, planning and preparing for formal meetings with regulatory agencies and interpreting HA feedback from these interactions.
- Experience providing hands-on support for planning clinical trial and marketing applications to health authorities including but not limited to FDA, EMA
Company info
- This position works cross-functionally with regulatory affairs and clinical development organizations to facilitate the completion of regulatory filing documentation according to company timelines.
- Ability to work independently as well as part of a team environment
This listing is sourced directly from Nurix Therapeutics's careers page and normalized into a canonical job model.