Senior Medical Director, Hematology
Pfizer
August 29, 2026
Remote friendly (Pennsylvania, United States)
United States
Medical Affairs
What You Will Achieve
In this role, you will:
- Serve as the Clinical Development Lead on subteams including Marketing Authorization Applications.
- Conduct medical monitoring (eligibility assessment, data review, safety monitoring).
- Lead peer-to-peer interactions with investigators; serve as point of contact for clinical issues between study teams and investigators.
- Lead and contribute to development/maintenance of clinical trial and regulatory documents with the Clinical Scientist and cross-functional team.
- Collaborate with the Global Development Team to create/refine development strategies.
- Represent the company in external engagements or 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 latest developments, literature, and guidelines to advise and drive current/future clinical development plans.
What You Will Need (Basic Qualifications):
- Medical degree with 5+ years clinical/industry experience.
- Hematology/Oncology clinical experience (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 oncology drug classes.
- Late clinical development experience in hematology.
Benefits/Work Location (if applicable):
- Hybrid role; live within commuting distance and work on-site ~2.5 days/week.
- Eligible for Global Performance Plan bonus (25% target) and share-based long-term incentives; comprehensive benefits incl. 401(k), paid time off, caregiver/parental and medical leave, and health coverage.
In this role, you will:
- Serve as the Clinical Development Lead on subteams including Marketing Authorization Applications.
- Conduct medical monitoring (eligibility assessment, data review, safety monitoring).
- Lead peer-to-peer interactions with investigators; serve as point of contact for clinical issues between study teams and investigators.
- Lead and contribute to development/maintenance of clinical trial and regulatory documents with the Clinical Scientist and cross-functional team.
- Collaborate with the Global Development Team to create/refine development strategies.
- Represent the company in external engagements or 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 latest developments, literature, and guidelines to advise and drive current/future clinical development plans.
What You Will Need (Basic Qualifications):
- Medical degree with 5+ years clinical/industry experience.
- Hematology/Oncology clinical experience (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 oncology drug classes.
- Late clinical development experience in hematology.
Benefits/Work Location (if applicable):
- Hybrid role; live within commuting distance and work on-site ~2.5 days/week.
- Eligible for Global Performance Plan bonus (25% target) and share-based long-term incentives; comprehensive benefits incl. 401(k), paid time off, caregiver/parental and medical leave, and health coverage.