Clinical Development Senior Medical Director, Breast Oncology
Pfizer
July 01, 2026
Remote friendly (La Jolla, CA)
United States
Clinical Research and Development
Job Responsibilities
- Conduct medical monitoring: eligibility assessment, data review, and safety monitoring.
- Lead peer-to-peer interactions with investigators.
- Serve as point of contact for clinical issues among study team, investigators, ethics committees, steering committees, and regulatory authorities.
- Lead and contribute to development/maintenance of clinical trial and regulatory documents with Clinical Scientist and cross-functional team.
- 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 or joint collaborations.
- Collaborate with Clinical Scientists to review/interpret clinical data, identify key findings and implications, and communicate to stakeholders.
- Stay current on literature/guidelines to advise and drive current/future 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; demonstrated diverse leadership (influence, coaching, guiding colleagues, business impact).
Work/Travel
- 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/Compensation
- Base salary range: $274,500–$457,500; eligible for bonus (25%) and long-term incentive; benefits include 401(k) match, paid time off, and medical/dental/vision.
Application Instructions
- Not specified in the provided text.
- Conduct medical monitoring: eligibility assessment, data review, and safety monitoring.
- Lead peer-to-peer interactions with investigators.
- Serve as point of contact for clinical issues among study team, investigators, ethics committees, steering committees, and regulatory authorities.
- Lead and contribute to development/maintenance of clinical trial and regulatory documents with Clinical Scientist and cross-functional team.
- 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 or joint collaborations.
- Collaborate with Clinical Scientists to review/interpret clinical data, identify key findings and implications, and communicate to stakeholders.
- Stay current on literature/guidelines to advise and drive current/future 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; demonstrated diverse leadership (influence, coaching, guiding colleagues, business impact).
Work/Travel
- 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/Compensation
- Base salary range: $274,500–$457,500; eligible for bonus (25%) and long-term incentive; benefits include 401(k) match, paid time off, and medical/dental/vision.
Application Instructions
- Not specified in the provided text.