Medical Director / Senior Medical Director
Nurix Therapeutics
September 03, 2026
On-site
Brisbane, CA
Medical Affairs
Job Responsibilities:
- Participate in, contribute to, and/or lead cross-functional clinical development teams; address study/program questions.
- Develop and implement global development plans.
- Review and author clinical protocols; interpret scientific/medical literature for clinical documents and decisions.
- 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 high-quality studies; support site/CRA training.
- Contribute to study concept/protocol development; coordinate final protocol and informed consent documents.
- Review medical data review plans and DSMB/SRC charters; contribute to study manuals and investigator materials.
- Develop CRFs and data edit checks; support ongoing data cleaning, reconciliation, and data trend analysis.
- Lead internal clinical data review meetings; support dose escalation meeting preparation.
- Coordinate external medical advisory committees (DSMBs/Scientific Steering Committees).
- Support literature review/training materials; contribute to statistical analysis plans and study data presentations.
- Address investigator questions; attend site initiation visits.
- Train other clinical scientists; medical monitoring duties may be considered.
- Support business development as scientific/SME.
- Up to 25% travel.
Basic Qualifications:
- MD, PhD, or PharmD (preferred); 15+ years (Executive Director) relevant drug development experience, including 5+ years in oncology clinical trials.
Preferred Qualifications/Skills:
- Clinical science experience in oncology (FIH/PoC) for small molecules, biologics and/or cell therapy; Phase 3/registrational desired.
- Strong clinical operations and translational medicine knowledge; excellent communication.
- Proficient in Microsoft Office; Spotfire/Medidata Rave (ideal).
- Strong ICH GCP understanding; patient safety and compliance commitment.
Compensation & Location:
- Salary range: $285,000–$390,000. Location: Brisbane, CA (onsite).
- Participate in, contribute to, and/or lead cross-functional clinical development teams; address study/program questions.
- Develop and implement global development plans.
- Review and author clinical protocols; interpret scientific/medical literature for clinical documents and decisions.
- 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 high-quality studies; support site/CRA training.
- Contribute to study concept/protocol development; coordinate final protocol and informed consent documents.
- Review medical data review plans and DSMB/SRC charters; contribute to study manuals and investigator materials.
- Develop CRFs and data edit checks; support ongoing data cleaning, reconciliation, and data trend analysis.
- Lead internal clinical data review meetings; support dose escalation meeting preparation.
- Coordinate external medical advisory committees (DSMBs/Scientific Steering Committees).
- Support literature review/training materials; contribute to statistical analysis plans and study data presentations.
- Address investigator questions; attend site initiation visits.
- Train other clinical scientists; medical monitoring duties may be considered.
- Support business development as scientific/SME.
- Up to 25% travel.
Basic Qualifications:
- MD, PhD, or PharmD (preferred); 15+ years (Executive Director) relevant drug development experience, including 5+ years in oncology clinical trials.
Preferred Qualifications/Skills:
- Clinical science experience in oncology (FIH/PoC) for small molecules, biologics and/or cell therapy; Phase 3/registrational desired.
- Strong clinical operations and translational medicine knowledge; excellent communication.
- Proficient in Microsoft Office; Spotfire/Medidata Rave (ideal).
- Strong ICH GCP understanding; patient safety and compliance commitment.
Compensation & Location:
- Salary range: $285,000–$390,000. Location: Brisbane, CA (onsite).