Clinical Development Medical Director, Breast Oncology
Pfizer
August 17, 2026
Remote friendly (Bothell, WA)
United States
Clinical Research and Development
Job Summary
This position is for a Clinical Development Medical Director within the prifetrastat program. This individual contributor supports clinical trials and leads clinical development subteams to ensure the program meets scientific, ethical, and regulatory standards.
Job Responsibilities
- Conduct medical monitoring activities including eligibility assessment, data review, and safety monitoring
- Lead peer-to-peer interactions with investigators
- Serve as the point of contact for clinical issues among study teams, investigators, ethics committees, steering committees, and regulatory authorities
- Lead and contribute to development and maintenance of clinical trial and regulatory documents in collaboration with Clinical Scientist and the cross-functional team
- Provide clinical development leadership across several study teams
- Serve as the Clinical Development representative on subteams, including for Marketing Authorization Applications
- Collaborate with the Global Development Team to create and refine development strategies
- Represent the company in external engagements or as a committee member in joint collaborations
- Collaborate with Clinical Scientists to review and interpret clinical data; identify key findings and implications; communicate to internal and external stakeholders
- Maintain clinical expertise by staying current with literature and guidelines to advise on current and future clinical development plans
Basic Qualifications
- Primary medical degree (MD, DO, MBBS, MBChB) from a recognized institution
- 4+ years of biopharmaceutical industry experience in clinical research and development
- Licensed by a licensing body/health authority to prescribe medicines independently for at least 2 years post intern/house officer/foundation period
Preferred Qualifications
- Board certified/eligible in oncology (or equivalent)
- Breast Oncology experience (2+ years)
- Late phase clinical development experience
Benefits (if stated)
- Participation in Pfizer’s Global Performance Plan (bonus target 25% of base salary) and eligibility for share-based long-term incentive
- Comprehensive benefits including medical, dental, vision, 401(k) with company match, paid vacation/holidays, and paid caregiver/parental and medical leave
Work Requirements
- Travel to scientific conferences/meetings several times per year as needed
- Hybrid role: live within commuting distance; work on-site ~2.5 days/week
Relocation
- Relocation support may be available
Application Instructions
- Not specified
This position is for a Clinical Development Medical Director within the prifetrastat program. This individual contributor supports clinical trials and leads clinical development subteams to ensure the program meets scientific, ethical, and regulatory standards.
Job Responsibilities
- Conduct medical monitoring activities including eligibility assessment, data review, and safety monitoring
- Lead peer-to-peer interactions with investigators
- Serve as the point of contact for clinical issues among study teams, investigators, ethics committees, steering committees, and regulatory authorities
- Lead and contribute to development and maintenance of clinical trial and regulatory documents in collaboration with Clinical Scientist and the cross-functional team
- Provide clinical development leadership across several study teams
- Serve as the Clinical Development representative on subteams, including for Marketing Authorization Applications
- Collaborate with the Global Development Team to create and refine development strategies
- Represent the company in external engagements or as a committee member in joint collaborations
- Collaborate with Clinical Scientists to review and interpret clinical data; identify key findings and implications; communicate to internal and external stakeholders
- Maintain clinical expertise by staying current with literature and guidelines to advise on current and future clinical development plans
Basic Qualifications
- Primary medical degree (MD, DO, MBBS, MBChB) from a recognized institution
- 4+ years of biopharmaceutical industry experience in clinical research and development
- Licensed by a licensing body/health authority to prescribe medicines independently for at least 2 years post intern/house officer/foundation period
Preferred Qualifications
- Board certified/eligible in oncology (or equivalent)
- Breast Oncology experience (2+ years)
- Late phase clinical development experience
Benefits (if stated)
- Participation in Pfizer’s Global Performance Plan (bonus target 25% of base salary) and eligibility for share-based long-term incentive
- Comprehensive benefits including medical, dental, vision, 401(k) with company match, paid vacation/holidays, and paid caregiver/parental and medical leave
Work Requirements
- Travel to scientific conferences/meetings several times per year as needed
- Hybrid role: live within commuting distance; work on-site ~2.5 days/week
Relocation
- Relocation support may be available
Application Instructions
- Not specified