Lead Medical Director, Product Development, Hematology
Core
Lead Medical Director responsible for developing and executing late-stage (Phase II–III) clinical strategies and plans for hematology/oncology molecules to deliver medically-differentiated therapies.
Role type
Senior IC medical director (clinical development)
Builds
Clinical Development Plans (CDP) and regulatory submissions for late-stage drug candidates
Domain
Biopharmaceuticals, Oncology & Hematology
Required skills
Board Certified/Eligible MD (MBBS) in Oncology & Hematology, Phase II–III drug development expertise, medical monitoring, clinical site/PI/KOL engagement, scientific writing, data analysis and interpretation
Preferred skills
Lymphoma disease area focus, outcome trial design experience, pharma/biotech industry knowledge
Technologies
None stated
Responsibilities
Develop and implement Clinical Development Plans (CDP), collaborate with internal/external stakeholders (business development, commercial, legal), provide clinical science input for Phase I–II protocols and regulatory filings, ensure strategic alignment of CDP with CD strategy, support senior team in medical monitoring
Seniority
Senior, hands-on IC