Medical Director

Job Summary

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