Clinical Development Medical Director, Hematology
Pfizer
August 25, 2026
Remote friendly (New York, NY)
United States
Clinical Research and Development
Job Summary
The Medical Director provides Clinical Development leadership and expertise on late-phase clinical trials, including overseeing design, conduct, and analysis within Hematology. Works with regulatory affairs, pharmacovigilance, biostatistics, and medical affairs to ensure scientific, ethical, and regulatory standards.
Responsibilities
- Provide clinical leadership across 2–3 study team(s) in collaboration 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 between study team, investigators, ethics committees, steering committees, and regulatory authorities.
- Lead and contribute to development/maintenance of clinical trial and regulatory documents.
- Review and interpret clinical data; identify key findings/implications and communicate to internal/external stakeholders.
- Stay current on literature, developments, and guidelines to advise and drive clinical development plans.
Basic Qualifications
- Clinical Development experience required.
- Medical Degree with 4+ years experience.
- Primary medical degree (MD, DO, MBBS, MBChB or equivalent).
- Licensed to prescribe independently for at least 2 years post intern/house officer/foundation.
Preferred Qualifications
- Late-stage clinical development experience.
- Hematology experience.
- Board certified/eligible in oncology (or equivalent).
Benefits (as stated)
- Bonus target 25% of base salary; participation in global performance plan and share-based long-term incentive.
- 401(k) with matching and additional retirement contribution; paid vacation/holidays/personal days; paid caregiver/parental and medical leave; medical/dental/vision coverage.
Work/Travel
- Hybrid: on-site ~2.5 days/week; travel ~4 times/year.
The Medical Director provides Clinical Development leadership and expertise on late-phase clinical trials, including overseeing design, conduct, and analysis within Hematology. Works with regulatory affairs, pharmacovigilance, biostatistics, and medical affairs to ensure scientific, ethical, and regulatory standards.
Responsibilities
- Provide clinical leadership across 2–3 study team(s) in collaboration 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 between study team, investigators, ethics committees, steering committees, and regulatory authorities.
- Lead and contribute to development/maintenance of clinical trial and regulatory documents.
- Review and interpret clinical data; identify key findings/implications and communicate to internal/external stakeholders.
- Stay current on literature, developments, and guidelines to advise and drive clinical development plans.
Basic Qualifications
- Clinical Development experience required.
- Medical Degree with 4+ years experience.
- Primary medical degree (MD, DO, MBBS, MBChB or equivalent).
- Licensed to prescribe independently for at least 2 years post intern/house officer/foundation.
Preferred Qualifications
- Late-stage clinical development experience.
- Hematology experience.
- Board certified/eligible in oncology (or equivalent).
Benefits (as stated)
- Bonus target 25% of base salary; participation in global performance plan and share-based long-term incentive.
- 401(k) with matching and additional retirement contribution; paid vacation/holidays/personal days; paid caregiver/parental and medical leave; medical/dental/vision coverage.
Work/Travel
- Hybrid: on-site ~2.5 days/week; travel ~4 times/year.