Clinical Development Medical Director, Breast Oncology
Pfizer
August 17, 2026
Remote friendly (San Diego, CA)
United States
Clinical Research and Development
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 between the study team, investigators, ethics committees, steering committees, and regulatory authorities.
- Lead and contribute to development and maintenance of clinical trial and regulatory documents (with Clinical Scientist and cross-functional team).
- Provide clinical development leadership across several study teams.
- Serve as the Clinical Development representative on subteams, including for Marketing Authorization Applications.
Strategic Guidance, Clinical Insights & Interpretation
- Collaborate with the Global Development Team to create and refine development strategies.
- Represent the company in external engagements or joint collaborations (as committee member).
- Collaborate with Clinical Scientists to review and interpret clinical data, identify key findings and implications, and communicate to internal/external stakeholders.
- Stay current with developments, literature, and guidelines to advise on and drive current/future clinical development plans.
Basic Qualifications
- Primary medical degree (MD/DO/MBBS/MBChB) from a recognized institution.
- 4+ years of experience in biopharmaceutical 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.
- Breast Oncology experience (2+ years).
- Late phase clinical development experience.
Benefits (if required)
- Eligible for participation in Pfizer’s Global Performance Plan with bonus target of 25% of base salary and share-based long-term incentive program.
- 401(k) with matching contributions and additional retirement savings contribution; paid vacation/holidays/personal days; paid caregiver/parental and medical leave; medical/dental/vision coverage.
Work Location / Schedule
- Hybrid: live within commuting distance; work on-site ~2.5 days/week.
- Travel to scientific conferences/meetings several times per year as needed.
Relocation
- Relocation support may be available.
Application instructions
- Apply via Pfizer Careers (U.S. benefits and role pay information provided on the candidate site).
- 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 between the study team, investigators, ethics committees, steering committees, and regulatory authorities.
- Lead and contribute to development and maintenance of clinical trial and regulatory documents (with Clinical Scientist and cross-functional team).
- Provide clinical development leadership across several study teams.
- Serve as the Clinical Development representative on subteams, including for Marketing Authorization Applications.
Strategic Guidance, Clinical Insights & Interpretation
- Collaborate with the Global Development Team to create and refine development strategies.
- Represent the company in external engagements or joint collaborations (as committee member).
- Collaborate with Clinical Scientists to review and interpret clinical data, identify key findings and implications, and communicate to internal/external stakeholders.
- Stay current with developments, literature, and guidelines to advise on and drive current/future clinical development plans.
Basic Qualifications
- Primary medical degree (MD/DO/MBBS/MBChB) from a recognized institution.
- 4+ years of experience in biopharmaceutical 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.
- Breast Oncology experience (2+ years).
- Late phase clinical development experience.
Benefits (if required)
- Eligible for participation in Pfizer’s Global Performance Plan with bonus target of 25% of base salary and share-based long-term incentive program.
- 401(k) with matching contributions and additional retirement savings contribution; paid vacation/holidays/personal days; paid caregiver/parental and medical leave; medical/dental/vision coverage.
Work Location / Schedule
- Hybrid: live within commuting distance; work on-site ~2.5 days/week.
- Travel to scientific conferences/meetings several times per year as needed.
Relocation
- Relocation support may be available.
Application instructions
- Apply via Pfizer Careers (U.S. benefits and role pay information provided on the candidate site).