Clinical Development Medical Director, Hematology
Pfizer
August 26, 2026
Remote friendly (San Diego, CA)
United States
Clinical Research and Development
Job Summary
The Medical Director provides Clinical Development leadership for late-phase hematology trials, overseeing study design, conduct, and analysis, and partnering cross-functionally (regulatory affairs, pharmacovigilance, biostatistics, medical affairs) to meet scientific, ethical, and regulatory standards.
Responsibilities
- Lead study-level clinical development across 2–3 study team(s) with Clinical Scientist(s).
- 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/steering committees, and regulatory authorities.
- Lead and contribute to clinical trial and regulatory document development/maintenance.
- Review/interpret clinical data, identify key findings/implications, and communicate internally/externally.
- Stay current on literature and guidelines to advise and drive present/future clinical development plans.
Qualifications
- Clinical Development experience required.
- Medical Degree with 4+ years experience.
- Primary medical degree (MD/DO/MBBS/MBChB) from recognized institution.
- Licensed to prescribe medicines independently for at least 2 years post intern/house officer/foundation.
Preferred Qualifications
- Late-stage clinical development; Hematology.
- Board certified/eligible in oncology (or equivalent).
Benefits / Work Requirements
- Hybrid role; live within commuting distance; on-site ~2.5 days/week. Travel ~4 times/year. Relocation assistance may be available.
- Eligible for Global Performance Plan bonus (target 25%) and long-term incentive program; comprehensive benefits including 401(k), paid leave, and health coverage.
The Medical Director provides Clinical Development leadership for late-phase hematology trials, overseeing study design, conduct, and analysis, and partnering cross-functionally (regulatory affairs, pharmacovigilance, biostatistics, medical affairs) to meet scientific, ethical, and regulatory standards.
Responsibilities
- Lead study-level clinical development across 2–3 study team(s) with Clinical Scientist(s).
- 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/steering committees, and regulatory authorities.
- Lead and contribute to clinical trial and regulatory document development/maintenance.
- Review/interpret clinical data, identify key findings/implications, and communicate internally/externally.
- Stay current on literature and guidelines to advise and drive present/future clinical development plans.
Qualifications
- Clinical Development experience required.
- Medical Degree with 4+ years experience.
- Primary medical degree (MD/DO/MBBS/MBChB) from recognized institution.
- Licensed to prescribe medicines independently for at least 2 years post intern/house officer/foundation.
Preferred Qualifications
- Late-stage clinical development; Hematology.
- Board certified/eligible in oncology (or equivalent).
Benefits / Work Requirements
- Hybrid role; live within commuting distance; on-site ~2.5 days/week. Travel ~4 times/year. Relocation assistance may be available.
- Eligible for Global Performance Plan bonus (target 25%) and long-term incentive program; comprehensive benefits including 401(k), paid leave, and health coverage.