Medical Monitor Director

Job Summary

To support clinical development programs, the remote contract Medical Monitor Director will manage the design, implementation, and evaluation of clinical study protocols while ensuring compliance with regulatory requirements and overseeing study integrity and safety data communication.

Key responsibilities:

• Oversees clinical studies, ensuring overall study integrity and compliance with Good Clinical Practice and safety standards
• Provides education and guidance to study personnel and collaborates with cross-functional teams to meet project deliverables
• Maintains expertise in therapeutic areas and participates in quality assurance activities, including audits and peer reviews

Required qualifications:

• Medical Doctor (M.D.) or Doctor of Osteopathy (D.O.) with relevant specialty experience and U.S. residency training preferred
• 5+ years of clinical trial experience, preferably in the pharmaceutical industry or academia
• Experience with Acute Leukemia and/or AML trials is preferred
• Demonstrated ability to interpret safety and efficacy data and manage risks effectively
• Familiarity with clinical trial methodology and regulatory compliance requirements