Global Development Medical Director, Hematology Oncology

Role: Global Development Medical Director in Hematology Oncology, responsible for leading clinical strategy, study design, and medical oversight of hematology-oncology programs from early to late-phase trials. Core responsibilities include contributing to clinical trial design, ensuring safety and ethical standards, providing medical monitoring, and supporting regulatory submissions for hematologic cancers with modalities including biologics and cell therapies. The role involves cross-functional collaboration within Clinical Project Teams, Global Study Teams, and external investigators, ensuring scientific rigor and compliance with GxP, GCP, and regulatory guidelines. Qualifications: MD or equivalent with at least 2 years of relevant clinical or research experience in oncology or hematology, preferably with board certification. Strong knowledge of clinical trial methodology, regulatory processes, and industry R&D operations is required. Preferred: Hemato-oncology clinical training, experience in biologics or cell therapy development, and prior involvement in regulatory submissions. High-value biopharma details include focus on hematological cancers, early- and late-phase clinical development, safety monitoring, regulatory documentation, and cross-disciplinary teamwork. Location: Boston, US.