Clinical Development Medical Director, Hematology

Role: Lead medical expertise and clinical development for late-phase hematology trials, ensuring scientific rigor and regulatory compliance. Responsibilities: oversee study design, conduct medical monitoring, interpret clinical data, and serve as liaison with investigators, regulatory bodies, and stakeholders. Provides strategic clinical insights, guides protocol development, and maintains expertise on current standards and guidelines. Requirements: Medical degree (MD, DO, MBBS, MBChB), 4+ years in clinical development, licensed to prescribe medicines independently for at least 2 years. Preferred: late-stage clinical development experience, hematology background, board certification or eligibility in oncology. High-Value: focus on hematology, late-phase trials, cross-functional collaboration, regulatory interactions, and clinical strategy. Work setup: hybrid role in the U.S., with approximately 4 annual travel; reporting to senior medical leadership.