Senior Medical Director Clinical Development - Prostate Cancer
Bristol Myers Squibb
August 07, 2026
Remote
United States
Clinical Research and Development
Responsibilities:
- Interact with clinical investigators and thought leaders to design clinical development plans for nominated drug candidates.
- Lead internal study teams; partner with investigators and CROs to design and implement clinical studies.
- Work with GPLs to ensure development and commercial optimization of RayzeBio assets.
- Contribute to protocols, investigator brochures, clinical study reports, and other clinical trial/regulatory documents.
- Conduct investigator meetings; lead site qualification and initiation visits.
- Execute and deploy drug development strategic plans; develop contingency plans; provide technical/strategic advice; meet milestones and budgets.
- Translate research and nonclinical findings into clinical development opportunities.
- Oversee Data Review and Independent Data Monitoring Committees.
- Conduct clinical trials using relevant pharmaceutical ethical guidelines and ensure compliance.
- Serve as clinical lead for regulatory interactions as needed; prepare briefing documents; attend/present at health authority meetings; oversee regulatory submissions.
- Lead cross-functional study teams; supervise and mentor clinical scientists and medical directors.
- Recruit, build, and manage medical directors and clinical scientists as needed.
- Leverage AI to drive program/portfolio/functional performance.
- Travel ~30%.
Education & Experience (Required):
- MD (or equivalent), ideally oncology subspecialty training; at least 10 years pharmaceutical/biotech/academic oncology solid tumor clinical development.
- Prostate cancer drug development experience.
Skills & Qualifications (Required/Preferred):
- Patient-focused; passion for novel therapeutics.
- Can-do, collegial leadership through influence; effective collaboration across functions.
- Ability to lead clinical/cross-functional teams; manage multiple stakeholders.
- Strong written/oral communication and presentation skills.
- Strong critical, strategic, analytical thinking.
- Experience with NDA/MAA preparation/submission and global health authority interactions.
- Protocol conduct experience (early and late phase), including writing, start-up, execution, analysis, reporting.
- Experience working with investigative sites.
- GCP/ICH understanding; ability to operate in a highly regulated environment and adhere to SOPs.
Benefits (Explicitly stated):
- Health coverage (medical, pharmacy, dental, vision); wellbeing support (EAP and related programs); 401(k), disability, life/accident insurance, supplemental health, business travel protection, legal support, survivor support.
- Paid time off: flexible time off (US Exempt Employees) or 160 hours annual paid vacation (Phoenix/AZ, Puerto Rico, exempt/non-exempt/hourly as stated); paid national holidays and optional holidays as stated; possible additional benefits based on eligibility.
Application instructions:
- If your resume doesn’t perfectly match, apply anyway.
- Interact with clinical investigators and thought leaders to design clinical development plans for nominated drug candidates.
- Lead internal study teams; partner with investigators and CROs to design and implement clinical studies.
- Work with GPLs to ensure development and commercial optimization of RayzeBio assets.
- Contribute to protocols, investigator brochures, clinical study reports, and other clinical trial/regulatory documents.
- Conduct investigator meetings; lead site qualification and initiation visits.
- Execute and deploy drug development strategic plans; develop contingency plans; provide technical/strategic advice; meet milestones and budgets.
- Translate research and nonclinical findings into clinical development opportunities.
- Oversee Data Review and Independent Data Monitoring Committees.
- Conduct clinical trials using relevant pharmaceutical ethical guidelines and ensure compliance.
- Serve as clinical lead for regulatory interactions as needed; prepare briefing documents; attend/present at health authority meetings; oversee regulatory submissions.
- Lead cross-functional study teams; supervise and mentor clinical scientists and medical directors.
- Recruit, build, and manage medical directors and clinical scientists as needed.
- Leverage AI to drive program/portfolio/functional performance.
- Travel ~30%.
Education & Experience (Required):
- MD (or equivalent), ideally oncology subspecialty training; at least 10 years pharmaceutical/biotech/academic oncology solid tumor clinical development.
- Prostate cancer drug development experience.
Skills & Qualifications (Required/Preferred):
- Patient-focused; passion for novel therapeutics.
- Can-do, collegial leadership through influence; effective collaboration across functions.
- Ability to lead clinical/cross-functional teams; manage multiple stakeholders.
- Strong written/oral communication and presentation skills.
- Strong critical, strategic, analytical thinking.
- Experience with NDA/MAA preparation/submission and global health authority interactions.
- Protocol conduct experience (early and late phase), including writing, start-up, execution, analysis, reporting.
- Experience working with investigative sites.
- GCP/ICH understanding; ability to operate in a highly regulated environment and adhere to SOPs.
Benefits (Explicitly stated):
- Health coverage (medical, pharmacy, dental, vision); wellbeing support (EAP and related programs); 401(k), disability, life/accident insurance, supplemental health, business travel protection, legal support, survivor support.
- Paid time off: flexible time off (US Exempt Employees) or 160 hours annual paid vacation (Phoenix/AZ, Puerto Rico, exempt/non-exempt/hourly as stated); paid national holidays and optional holidays as stated; possible additional benefits based on eligibility.
Application instructions:
- If your resume doesn’t perfectly match, apply anyway.