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
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Phase II–III drug development, clinical trial design, medical monitoring, scientific writing, data analysis, regulatory submission support, KOL engagement, strategic planning
Preferred skills
Lymphoma disease area focus, outcome trial design, pharma/biotech industry knowledge, cross-functional collaboration
Technologies
Clinical trial management systems, regulatory submission platforms
Responsibilities
Develop and implement Clinical Development Plans (CDP); collaborate with internal/external stakeholders on late-stage clinical strategies; provide clinical science input for regulatory filings; ensure strategic alignment of CDP with organizational goals; engage with clinical sites and KOLs; contribute to label-enabling outcomes
Seniority
Senior, hands-on IC
