Senior Medical Director, Hematology
Pfizer
August 29, 2026
Remote friendly (La Jolla, CA)
United States
Medical Affairs
What You Will Achieve
Clinical Development Leadership on Study Teams and Development Subteams
- Serve as Clinical Development Lead on subteams, including Marketing Authorization Applications.
- Conduct medical monitoring: eligibility assessment, data review, and safety monitoring.
- Lead peer-to-peer interactions with investigators.
- Be the point of contact for clinical issues between study teams and investigators.
- Lead and contribute to development and maintenance of clinical trial and regulatory documents with Clinical Scientists and cross-functional partners.
- Collaborate with the Global Development Team to create and refine development strategies.
- Represent the company in external engagements and committee/joint collaboration settings.
- Support regulatory interactions.
- Collaborate with Clinical Scientists to review and interpret clinical data; identify key findings and implications; communicate to internal and external stakeholders.
- Stay current with literature, guidelines, and developments to advise on 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 in academia/industry.
- Late-stage clinical development experience.
- Experience providing clinical development leadership across several study teams.
- Excellent communication skills for complex technical concepts.
- Strong strategic and analytical skills.
Bonus To Have (Preferred Qualifications)
- Leadership/management experience.
- Board certified/eligible in hematology/oncology.
- Experience across multiple phases and drug classes in oncology.
- Late clinical development experience in hematology.
Relocation support may be available.
Hybrid: live within commuting distance; work on-site ~2.5 days/week.
Clinical Development Leadership on Study Teams and Development Subteams
- Serve as Clinical Development Lead on subteams, including Marketing Authorization Applications.
- Conduct medical monitoring: eligibility assessment, data review, and safety monitoring.
- Lead peer-to-peer interactions with investigators.
- Be the point of contact for clinical issues between study teams and investigators.
- Lead and contribute to development and maintenance of clinical trial and regulatory documents with Clinical Scientists and cross-functional partners.
- Collaborate with the Global Development Team to create and refine development strategies.
- Represent the company in external engagements and committee/joint collaboration settings.
- Support regulatory interactions.
- Collaborate with Clinical Scientists to review and interpret clinical data; identify key findings and implications; communicate to internal and external stakeholders.
- Stay current with literature, guidelines, and developments to advise on 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 in academia/industry.
- Late-stage clinical development experience.
- Experience providing clinical development leadership across several study teams.
- Excellent communication skills for complex technical concepts.
- Strong strategic and analytical skills.
Bonus To Have (Preferred Qualifications)
- Leadership/management experience.
- Board certified/eligible in hematology/oncology.
- Experience across multiple phases and drug classes in oncology.
- Late clinical development experience in hematology.
Relocation support may be available.
Hybrid: live within commuting distance; work on-site ~2.5 days/week.