Global Development Medical Director, Hematology Oncology

Role: Global Development Medical Director in Hematology, based in Boston, with a hybrid work setup. Objectives include leading clinical development strategies for hematology-oncology assets, supporting early and late-phase trials, and ensuring regulatory compliance for product registration. Responsibilities encompass designing clinical protocols, providing medical oversight and safety monitoring, contributing to program strategy, and liaising with internal and external stakeholders including investigators and regulatory bodies. The role involves leading cross-functional teams within Clinical Project Teams and Study Teams, ensuring scientific rigor and ethical standards in clinical trials, and authoring regulatory documents such as INDs and NDAs. Qualifications require an MD or international equivalent with at least 2 years of relevant clinical or research experience, preferably in hemato-oncology, with board certification preferred. The candidate should possess knowledge of GCP, clinical trial methodology, and the regulatory landscape, along with strong communication skills. High-value specifics include focus on hematological cancers leveraging platforms like Immuno-Oncology, DNA Damage Response, and Cell Therapy, spanning early to late-stage development and regulatory submission activities. The position demands collaboration across R&D functions and external research sites, requiring strong leadership and strategic input in a global biopharma setting.