Clinical Development Senior Medical Director, Breast Oncology
Pfizer
August 30, 2026
Remote friendly (Cambridge, MA)
United States
Clinical Research and Development
Job Responsibilities
- Conduct medical monitoring activities: eligibility assessment, data review, and safety monitoring.
- Lead peer-to-peer interactions with investigators.
- Serve as point of contact for clinical issues between study team, investigators, ethics/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 Marketing Authorization Applications.
- Collaborate with Global Development Team to create/refine development strategies.
- Represent the company in external engagements/joint collaborations.
- Review and interpret clinical data with Clinical Scientists; communicate findings/implications to internal and external stakeholders.
- Stay abreast of latest literature/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 biopharma clinical research & development experience.
- Licensed by a health authority 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.
Work/Travel
- Hybrid; live within commuting distance; average ~2.5 onsite days/week.
- Travel to scientific meetings several times per year as needed.
Compensation/Benefits
- Base salary: $274,500–$457,500; bonus target 25% of base (Global Performance Plan) and eligible share-based long-term incentives; comprehensive benefits including 401(k) and health coverage.
- Conduct medical monitoring activities: eligibility assessment, data review, and safety monitoring.
- Lead peer-to-peer interactions with investigators.
- Serve as point of contact for clinical issues between study team, investigators, ethics/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 Marketing Authorization Applications.
- Collaborate with Global Development Team to create/refine development strategies.
- Represent the company in external engagements/joint collaborations.
- Review and interpret clinical data with Clinical Scientists; communicate findings/implications to internal and external stakeholders.
- Stay abreast of latest literature/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 biopharma clinical research & development experience.
- Licensed by a health authority 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.
Work/Travel
- Hybrid; live within commuting distance; average ~2.5 onsite days/week.
- Travel to scientific meetings several times per year as needed.
Compensation/Benefits
- Base salary: $274,500–$457,500; bonus target 25% of base (Global Performance Plan) and eligible share-based long-term incentives; comprehensive benefits including 401(k) and health coverage.