Medical Director / Senior Medical Director 5948-306
Nurix Therapeutics
September 03, 2026
On-site
Brisbane, CA
Medical Affairs
Responsibilities:
- Participate, contribute, and/or lead cross-functional clinical development teams to address study/program questions.
- Develop and implement the Global Development Plan with senior clinical development staff.
- Review and author clinical protocols; read and interpret scientific/medical literature to support 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, efficiently delivered studies.
- Support study concept and protocol development; coordinate final protocol and informed consent documents.
- Contribute to medical data review plans; DSMB/SRC charters; sections of study manuals and investigator materials.
- Develop CRFs and data edit checks; oversee data cleaning (queries, coding review, SAE reconciliation) and data trend analysis.
- Lead internal clinical data review meetings with the medical monitor; prepare for dose escalation meetings as applicable.
- Coordinate external advisory committees (DSMBs, Scientific Steering Committees) with the medical monitor.
- Research literature and prepare training materials; contribute to statistical analysis plans and study data presentations.
- Address investigator questions; attend site initiation visits (SIVs) with the medical monitor.
- Assist with functional area priority activities; train clinical scientists.
- Support medical monitoring duties as applicable; support business development as a scientific/SME.
- Up to 25% travel (US and international).
Qualifications:
- Advanced degree (MD, PhD, or PharmD preferred).
- 15+ years relevant drug development experience; minimum 5 years oncology clinical trials (Executive Director).
Preferred:
- Clinical science experience in oncology for first-in-human and proof of concept (small molecules, biologics, and/or cell therapy); registrational or Phase 3 desired.
- Deep clinical operations and translational medicine knowledge.
- Strong communication/interpersonal skills; able to translate technical concepts.
- Attention to detail; collaboration; deadline focus.
- Microsoft Office (Excel, Word, PowerPoint, OneNote); Spotfire and Medidata Rave (or similar) preferred.
- Strong ICH GCP understanding; industry standards knowledge.
- Commitment to patient safety and clinical compliance.
Location: Brisbane, CA (onsite).
- Participate, contribute, and/or lead cross-functional clinical development teams to address study/program questions.
- Develop and implement the Global Development Plan with senior clinical development staff.
- Review and author clinical protocols; read and interpret scientific/medical literature to support 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, efficiently delivered studies.
- Support study concept and protocol development; coordinate final protocol and informed consent documents.
- Contribute to medical data review plans; DSMB/SRC charters; sections of study manuals and investigator materials.
- Develop CRFs and data edit checks; oversee data cleaning (queries, coding review, SAE reconciliation) and data trend analysis.
- Lead internal clinical data review meetings with the medical monitor; prepare for dose escalation meetings as applicable.
- Coordinate external advisory committees (DSMBs, Scientific Steering Committees) with the medical monitor.
- Research literature and prepare training materials; contribute to statistical analysis plans and study data presentations.
- Address investigator questions; attend site initiation visits (SIVs) with the medical monitor.
- Assist with functional area priority activities; train clinical scientists.
- Support medical monitoring duties as applicable; support business development as a scientific/SME.
- Up to 25% travel (US and international).
Qualifications:
- Advanced degree (MD, PhD, or PharmD preferred).
- 15+ years relevant drug development experience; minimum 5 years oncology clinical trials (Executive Director).
Preferred:
- Clinical science experience in oncology for first-in-human and proof of concept (small molecules, biologics, and/or cell therapy); registrational or Phase 3 desired.
- Deep clinical operations and translational medicine knowledge.
- Strong communication/interpersonal skills; able to translate technical concepts.
- Attention to detail; collaboration; deadline focus.
- Microsoft Office (Excel, Word, PowerPoint, OneNote); Spotfire and Medidata Rave (or similar) preferred.
- Strong ICH GCP understanding; industry standards knowledge.
- Commitment to patient safety and clinical compliance.
Location: Brisbane, CA (onsite).