Clinical Development Senior Medical Director, Breast Oncology
Pfizer
July 02, 2026
Remote friendly (Cambridge, MA)
United States
Clinical Research and Development
Job Responsibilities
- Conduct medical monitoring (eligibility assessment, data review, 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/contribute to development and maintenance of clinical trial and regulatory documents with Clinical Scientists and cross-functional teams.
- Provide clinical development leadership across several study teams.
- Serve as Clinical Development Lead on subteams, including for Marketing Authorization Applications.
Strategic Guidance, Clinical Insights & Interpretation
- Collaborate with Global Development Team to create/refine development strategies.
- Represent the company in external engagements/joint collaborations.
- Collaborate with Clinical Scientists to review and interpret data, identify key findings/implications, and communicate to internal/external stakeholders.
- Stay current with literature and guidelines to advise and drive clinical development plans.
Basic Qualifications
- Medical degree with 5+ years industry experience.
- Clinical oncology experience (typically 4+ years).
Preferred Qualifications
- Board certified/eligible in oncology (or equivalent).
- Breast Oncology experience (2+ years).
- Late-phase clinical development experience.
Work/Environment
- Travel to scientific conferences/meetings several times per year.
- Hybrid: live within commuting distance; work on-site ~2.5 days/week. Relocation support available.
Benefits (as stated)
- 401(k) with matching and additional retirement contribution; paid vacation/holidays/personal days; caregiver/parental and medical leave; medical/prescription/dental/vision coverage.
- Conduct medical monitoring (eligibility assessment, data review, 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/contribute to development and maintenance of clinical trial and regulatory documents with Clinical Scientists and cross-functional teams.
- Provide clinical development leadership across several study teams.
- Serve as Clinical Development Lead on subteams, including for Marketing Authorization Applications.
Strategic Guidance, Clinical Insights & Interpretation
- Collaborate with Global Development Team to create/refine development strategies.
- Represent the company in external engagements/joint collaborations.
- Collaborate with Clinical Scientists to review and interpret data, identify key findings/implications, and communicate to internal/external stakeholders.
- Stay current with literature and guidelines to advise and drive clinical development plans.
Basic Qualifications
- Medical degree with 5+ years industry experience.
- Clinical oncology experience (typically 4+ years).
Preferred Qualifications
- Board certified/eligible in oncology (or equivalent).
- Breast Oncology experience (2+ years).
- Late-phase clinical development experience.
Work/Environment
- Travel to scientific conferences/meetings several times per year.
- Hybrid: live within commuting distance; work on-site ~2.5 days/week. Relocation support available.
Benefits (as stated)
- 401(k) with matching and additional retirement contribution; paid vacation/holidays/personal days; caregiver/parental and medical leave; medical/prescription/dental/vision coverage.