Nurix Therapeutics
Associate Director, Regulatory & Medical Writing
Brisbane, California · 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.
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About the role
- Investigator's brochures and annual updates
Responsibilities
- Manage the author, review, and approval process for multiple deliverables at a given time; ensure quality and timely completion, with attention to consistency of content, messaging, format, and style
- 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.
Requirements
- ability to meet day-to-day challenges with confidence and professionalism
- Proficiency in project planning tools such as MS Project or Smartsheet, collaborative authoring or document review tools, and Veeva RIM Suite
Nice to have
- Clinical study protocols and clinical protocol amendments
- Clinical study reports
- Lay-person summaries
- Integrated summary reports
- Clinical, nonclinical, and multidisciplinary information amendments
- NDA, BLA, MAA, and (e)CTD submissions
- Risk Management Plans
- ensure quality and timely completion, with attention to consistency of content, messaging, format, and style
Skills
- Excellent communication skills, organizational skills, and attention to detail
Compensation
- $216,400 - $234,800
Benefits
- Manage external Regulatory & Medical Writing resources for assigned programs/projects, as needed
This listing is sourced directly from Nurix Therapeutics's careers page and normalized into a canonical job model.