Medical Director

To oversee clinical studies and ensure compliance with safety and efficacy standards, the part-time contract Medical Director will manage study protocols, monitor study integrity, and collaborate with cross-functional teams while working remotely. Key responsibilities Manage the design, implementation, and evaluation of clinical study protocols in alignment with the Product Development Plan Oversee study enrollment, timelines, and deliverables while assessing and reporting serious adverse events Provide education and training for investigators and study site personnel, ensuring compliance with Good Clinical Practice and regulatory standards Required qualifications Medical Doctor (M.D.), Doctor of Osteopathy (D.O.), or equivalent degree with relevant therapeutic specialty experience 5+ years of clinical trial experience, preferably in the pharmaceutical industry or academia Experience with Acute Leukemia and/or AML trials is preferred Knowledge of clinical trial methodology and regulatory compliance requirements Proven ability to collaborate effectively in a cross-functional environment