Senior Medical Director, Hematology Clinical Development

Role: Lead clinical development activities for one or more therapeutic programs, overseeing trial design, execution, and data interpretation to support product strategy. Responsibilities: manage clinical trial planning and implementation, ensure regulatory compliance, oversee study timelines and safety reporting, contribute to scientific documentation (protocols, reports), and provide clinical expertise to cross-functional teams. May supervise Medical and Scientific Directors, participate in clinical strategy teams, and liaise with external opinion leaders. Requirements: MD or DO with at least 2 years of industry or academic clinical trial experience; strong understanding of clinical trial methodology, regulatory standards, and GxP. Preferred: subspecialty fellowship, experience in immunology, oncology, or neuroscience therapeutic areas, and experience in global clinical trials. High-Value: clinical trial oversight in immunology, oncology, or neuroscience; early to late-stage development, with responsibilities spanning from protocol design to regulatory interactions. Work setup: not specified; travel details not provided.