Senior Medical Director, Hematology
Pfizer
August 24, 2026
Remote friendly (La Jolla, CA)
United States
Medical Affairs
Senior Medical Director (Hematology) – Individual Contributor
What You Will Achieve
- Serve as Clinical Development Lead on subteams, including for Marketing Authorization Applications.
- Conduct medical monitoring: eligibility assessment, data review, and safety monitoring.
- Lead peer-to-peer interactions with investigators; act as point of contact for clinical issues between study team and investigators.
- Lead and contribute to development/maintenance of clinical trial and regulatory documents with Clinical Scientist and cross-functional team.
- Collaborate with Global Development Team to create/refine development strategies.
- Represent the company in external engagements and committee/joint collaborations.
- Support regulatory interactions.
- Collaborate with Clinical Scientist to review/interpret clinical data, identify key findings/implications, and communicate to internal/external stakeholders.
- Stay current with literature and guidelines to advise and drive current/future clinical development plans.
What You Will Need (Basic Qualifications)
- Medical degree; 5+ years clinical/industry experience.
- Hematology/Oncology clinical experience in academia/industry.
- Late-stage clinical development experience.
- Experience providing clinical development leadership across several study teams.
- Excellent communication skills; strong strategic and analytical skills.
Bonus To Have (Preferred Qualifications)
- Leadership/management experience.
- Board certified/eligible in hematology/oncology.
- Experience across multiple phases and across oncology drug classes.
- Late clinical development experience in hematology.
Work Location
- Hybrid: live within commuting distance; work on-site ~2.5 days/week. Relocation support may be available.
Benefits/Compensation (as stated)
- Base salary range: $274,500–$457,500; bonus target 25% of base; eligibility for share-based long-term incentive; comprehensive benefits including 401(k) with matching, paid leave, and medical/dental/vision coverage.
What You Will Achieve
- Serve as Clinical Development Lead on subteams, including for Marketing Authorization Applications.
- Conduct medical monitoring: eligibility assessment, data review, and safety monitoring.
- Lead peer-to-peer interactions with investigators; act as point of contact for clinical issues between study team and investigators.
- Lead and contribute to development/maintenance of clinical trial and regulatory documents with Clinical Scientist and cross-functional team.
- Collaborate with Global Development Team to create/refine development strategies.
- Represent the company in external engagements and committee/joint collaborations.
- Support regulatory interactions.
- Collaborate with Clinical Scientist to review/interpret clinical data, identify key findings/implications, and communicate to internal/external stakeholders.
- Stay current with literature and guidelines to advise and drive current/future clinical development plans.
What You Will Need (Basic Qualifications)
- Medical degree; 5+ years clinical/industry experience.
- Hematology/Oncology clinical experience in academia/industry.
- Late-stage clinical development experience.
- Experience providing clinical development leadership across several study teams.
- Excellent communication skills; strong strategic and analytical skills.
Bonus To Have (Preferred Qualifications)
- Leadership/management experience.
- Board certified/eligible in hematology/oncology.
- Experience across multiple phases and across oncology drug classes.
- Late clinical development experience in hematology.
Work Location
- Hybrid: live within commuting distance; work on-site ~2.5 days/week. Relocation support may be available.
Benefits/Compensation (as stated)
- Base salary range: $274,500–$457,500; bonus target 25% of base; eligibility for share-based long-term incentive; comprehensive benefits including 401(k) with matching, paid leave, and medical/dental/vision coverage.