Senior Medical Director Clinical Development - Prostate Cancer
Bristol Myers Squibb
August 29, 2026
Remote
United States
Clinical Research and Development
Responsibilities:
- Develop and execute clinical development strategy for prostate cancer assets from IND through Phase 3 registrational studies.
- Lead internal study teams; partner with investigators and CROs to design and implement clinical studies.
- Work with GPLs to support development and commercial optimization of assets.
- Contribute to protocols, investigator brochures, clinical study reports, and other trial/regulatory documents.
- Conduct investigator meetings; lead site qualification and initiation visits.
- Execute drug development strategic plans; develop contingency plans; advise technically/strategically; meet milestones and budgets.
- Translate research/nonclinical findings into clinical development opportunities.
- Oversee data review and Independent Data Monitoring Committees.
- Ensure trials follow relevant ethical guidelines and external compliance requirements.
- Lead regulatory interactions as needed (briefing documents; attend/present at health authority meetings); oversee regulatory submissions.
- Recruit, build, and manage medical directors and clinical scientists; supervise and mentor clinical scientists/medical directors.
- Leverage AI to improve program/portfolio/function performance; travel ~30%.
Qualifications:
- MD or equivalent; sub-specialty oncology training; 10+ years oncology solid tumor clinical development (radiopharmaceutical experience preferred).
- Required: prostate cancer drug development experience.
Skills/Requirements (selected):
- Patient-focused; strong collaboration and leadership; ability to manage multi-stakeholder engagements.
- Strong written/oral communication and presentation skills.
- Strategic/analytical thinking; GCP/ICH knowledge.
- Experience with NDA/MAA preparation/submission and global health authority interactions.
- Experience across protocol conduct (early/late phase), study startup, execution, analysis, reporting; site working experience.
- Ability to function in a highly regulated environment; adhere to RayzeBio guidelines/SOPs.
Compensation/Benefits (as stated):
- Remote (US): $306,814–$371,787; additional incentive cash/stock may be available.
- Benefits include medical/dental/vision; wellbeing support; 401(k); disability and life insurance; PTO (flexible time off or annual vacation depending on location/role).
- Develop and execute clinical development strategy for prostate cancer assets from IND through Phase 3 registrational studies.
- Lead internal study teams; partner with investigators and CROs to design and implement clinical studies.
- Work with GPLs to support development and commercial optimization of assets.
- Contribute to protocols, investigator brochures, clinical study reports, and other trial/regulatory documents.
- Conduct investigator meetings; lead site qualification and initiation visits.
- Execute drug development strategic plans; develop contingency plans; advise technically/strategically; meet milestones and budgets.
- Translate research/nonclinical findings into clinical development opportunities.
- Oversee data review and Independent Data Monitoring Committees.
- Ensure trials follow relevant ethical guidelines and external compliance requirements.
- Lead regulatory interactions as needed (briefing documents; attend/present at health authority meetings); oversee regulatory submissions.
- Recruit, build, and manage medical directors and clinical scientists; supervise and mentor clinical scientists/medical directors.
- Leverage AI to improve program/portfolio/function performance; travel ~30%.
Qualifications:
- MD or equivalent; sub-specialty oncology training; 10+ years oncology solid tumor clinical development (radiopharmaceutical experience preferred).
- Required: prostate cancer drug development experience.
Skills/Requirements (selected):
- Patient-focused; strong collaboration and leadership; ability to manage multi-stakeholder engagements.
- Strong written/oral communication and presentation skills.
- Strategic/analytical thinking; GCP/ICH knowledge.
- Experience with NDA/MAA preparation/submission and global health authority interactions.
- Experience across protocol conduct (early/late phase), study startup, execution, analysis, reporting; site working experience.
- Ability to function in a highly regulated environment; adhere to RayzeBio guidelines/SOPs.
Compensation/Benefits (as stated):
- Remote (US): $306,814–$371,787; additional incentive cash/stock may be available.
- Benefits include medical/dental/vision; wellbeing support; 401(k); disability and life insurance; PTO (flexible time off or annual vacation depending on location/role).