Clinical Development Medical Director, Breast Oncology
Pfizer
August 17, 2026
Remote friendly (Pennsylvania, United States)
United States
Clinical Research and Development
Clinical Development Medical Director (prifetrastat program)
Responsibilities
- Conduct medical monitoring activities including eligibility assessment, data review, and safety monitoring.
- Lead peer-to-peer interactions with investigators.
- Serve as point of contact for clinical issues among study teams, investigators, ethics committees, steering committees, and regulatory authorities.
- Lead and contribute to development/maintenance of clinical trial and regulatory documents with Clinical Scientists and cross-functional teams.
- Provide clinical development leadership across several study teams.
- Represent Clinical Development on subteams including for Marketing Authorization Applications.
- Collaborate with Global Development to create/refine development strategies.
- Represent the company in external engagements/joint collaborations.
- Collaborate with Clinical Scientists to review/interpret clinical data, identify key findings, and communicate to stakeholders.
- Stay current with literature and guidelines to advise and drive current/future clinical development plans.
Basic Qualifications
- Primary medical degree (MD, DO, MBBS, MBChB) from a recognized school.
- 4+ years biopharmaceutical clinical research & development experience.
- Licensed to prescribe medicines independently for at least 2 years post intern/house officer/foundation.
Preferred Qualifications
- Board certified/eligible in oncology (or equivalent).
- Breast oncology experience (2+ years).
- Late phase clinical development experience.
Travel/Location & Benefits
- Hybrid: live within commuting distance; work onsite ~2.5 days/week.
- Travel to scientific conferences/meetings several times per year.
- Relocation support may be available.
- Eligible for Global Performance Plan bonus (25% target) and share-based long-term incentive; comprehensive benefits including 401(k), paid time off, caregiver/parental and medical leave, and medical/dental/vision.
Responsibilities
- Conduct medical monitoring activities including eligibility assessment, data review, and safety monitoring.
- Lead peer-to-peer interactions with investigators.
- Serve as point of contact for clinical issues among study teams, investigators, ethics committees, steering committees, and regulatory authorities.
- Lead and contribute to development/maintenance of clinical trial and regulatory documents with Clinical Scientists and cross-functional teams.
- Provide clinical development leadership across several study teams.
- Represent Clinical Development on subteams including for Marketing Authorization Applications.
- Collaborate with Global Development to create/refine development strategies.
- Represent the company in external engagements/joint collaborations.
- Collaborate with Clinical Scientists to review/interpret clinical data, identify key findings, and communicate to stakeholders.
- Stay current with literature and guidelines to advise and drive current/future clinical development plans.
Basic Qualifications
- Primary medical degree (MD, DO, MBBS, MBChB) from a recognized school.
- 4+ years biopharmaceutical clinical research & development experience.
- Licensed to prescribe medicines independently for at least 2 years post intern/house officer/foundation.
Preferred Qualifications
- Board certified/eligible in oncology (or equivalent).
- Breast oncology experience (2+ years).
- Late phase clinical development experience.
Travel/Location & Benefits
- Hybrid: live within commuting distance; work onsite ~2.5 days/week.
- Travel to scientific conferences/meetings several times per year.
- Relocation support may be available.
- Eligible for Global Performance Plan bonus (25% target) and share-based long-term incentive; comprehensive benefits including 401(k), paid time off, caregiver/parental and medical leave, and medical/dental/vision.