Clinical Development Medical Director, Hematology

Role: Medical Director overseeing late-phase clinical trials in Hematology, providing clinical leadership, expertise, and strategic guidance throughout study design, conduct, and data interpretation. Responsibilities include medical monitoring, investigator interactions, and cross-functional collaboration with regulatory, pharmacovigilance, biostatistics, and medical affairs teams, ensuring compliance with scientific, ethical, and regulatory standards. The candidate offers medical insights, reviews clinical data, and contributes to regulatory documents. Requirements: Medical degree (MD, DO, MBBS, MBChB), 4+ years of clinical development experience, licensed to prescribe medicines for at least 2 years. Preferred: late-stage clinical experience, hematology background, board certification in oncology or related fields. The role involves partnering with study teams, reporting to senior medical leadership, and engaging with external stakeholders such as health authorities and ethics committees. Location: Hybrid, requiring onsite presence ~2.5 days/week, with travel (~4 times/year). High-value specifics include focus on hematology, late-phase trials, and regulatory interactions in a global pharma setting.