Medical Director / Senior Medical Director
Nurix Therapeutics
September 03, 2026
On-site
Brisbane, CA
Medical Affairs
Role Responsibilities:
- Participate in, contribute to, and/or lead cross-functional clinical development teams; address study/program questions.
- Develop and implement the Global Development Plan with senior clinical development staff.
- Review and author clinical protocols; interpret scientific/medical literature for clinical documents and team decision-making.
- Prepare clinical portions of regulatory filings and meeting packages (INDs, Annual Reports, meeting requests, NDAs) for US and ex-US authorities.
- Translate clinical research plans into efficiently delivered, high-quality studies.
- Support study concept/protocol development using clinical trial design and disease indication knowledge; coordinate final protocol and informed consent documents.
- Contribute to medical data review plans, DSMB/SRC charters, and sections of study manuals/investigator materials.
- Develop CRFs, data edit checks, patient profile design; perform ongoing data cleaning and data trend analysis.
- Lead internal clinical data review meetings; support dose escalation data preparation as applicable.
- Coordinate external medical advisory committees (e.g., DSMBs, Scientific Steering Committees).
- Research/summarize literature for continuous learning and training materials.
- Support statistical analysis plans, visual design (tables/listings/figures), and preparation of manuscripts/presentations.
- Address investigator questions; attend site initiation visits (SIVs) with the medical monitor.
- Train clinical scientists as needed.
- Support safety oversight; may include medical monitoring depending on degree/experience.
- Support business development as a scientific/subject-matter expert; up to 25% travel (US/International).
Qualifications:
- Advanced degree in clinical or biological sciences (MD, PhD, or PharmD preferred).
- 15+ years (Executive Director) relevant drug development experience; minimum 5 years in oncology clinical trials.
Preferred Qualifications/Skills:
- Experience in clinical science roles for oncology first-in-human/proof-of-concept; registrational or Phase 3 experience desired.
- Strong clinical operations and translational medicine knowledge; excellent communication/interpersonal skills.
- Ability to translate technical concepts for study teams; attention to detail, collaboration, initiative, and deadline management.
- Proficient with Microsoft Office; ideally Spotfire and Medidata Rave (or similar).
- Strong ICH GCP knowledge and industry standards; commitment to patient safety/clinical compliance.
Location/Work Setting:
- Brisbane, CA (Onsite).
Salary Range:
- $285,000 to $390,000
- Participate in, contribute to, and/or lead cross-functional clinical development teams; address study/program questions.
- Develop and implement the Global Development Plan with senior clinical development staff.
- Review and author clinical protocols; interpret scientific/medical literature for clinical documents and team decision-making.
- Prepare clinical portions of regulatory filings and meeting packages (INDs, Annual Reports, meeting requests, NDAs) for US and ex-US authorities.
- Translate clinical research plans into efficiently delivered, high-quality studies.
- Support study concept/protocol development using clinical trial design and disease indication knowledge; coordinate final protocol and informed consent documents.
- Contribute to medical data review plans, DSMB/SRC charters, and sections of study manuals/investigator materials.
- Develop CRFs, data edit checks, patient profile design; perform ongoing data cleaning and data trend analysis.
- Lead internal clinical data review meetings; support dose escalation data preparation as applicable.
- Coordinate external medical advisory committees (e.g., DSMBs, Scientific Steering Committees).
- Research/summarize literature for continuous learning and training materials.
- Support statistical analysis plans, visual design (tables/listings/figures), and preparation of manuscripts/presentations.
- Address investigator questions; attend site initiation visits (SIVs) with the medical monitor.
- Train clinical scientists as needed.
- Support safety oversight; may include medical monitoring depending on degree/experience.
- Support business development as a scientific/subject-matter expert; up to 25% travel (US/International).
Qualifications:
- Advanced degree in clinical or biological sciences (MD, PhD, or PharmD preferred).
- 15+ years (Executive Director) relevant drug development experience; minimum 5 years in oncology clinical trials.
Preferred Qualifications/Skills:
- Experience in clinical science roles for oncology first-in-human/proof-of-concept; registrational or Phase 3 experience desired.
- Strong clinical operations and translational medicine knowledge; excellent communication/interpersonal skills.
- Ability to translate technical concepts for study teams; attention to detail, collaboration, initiative, and deadline management.
- Proficient with Microsoft Office; ideally Spotfire and Medidata Rave (or similar).
- Strong ICH GCP knowledge and industry standards; commitment to patient safety/clinical compliance.
Location/Work Setting:
- Brisbane, CA (Onsite).
Salary Range:
- $285,000 to $390,000