Medical Director (Contract)

This part-time, contract opportunity is designed for a physician or PhD-level professional with expertise in endocrinology and clinical research. The Medical Director will provide strategic medical leadership across clinical trial projects, supporting study design, medical monitoring, regulatory activities, and data review. The role offers exposure to projects spanning early-phase through Phase III clinical development. You’ll contribute to protocol development, medical writing, FDA interactions, and the management of key safety and compliance activities. Working remotely and on an hourly, project-based schedule, you’ll collaborate with clinical and medical teams while operating with a high degree of independence. The position is well suited to an experienced clinical research professional who can provide strong therapeutic and regulatory expertise when projects require it.

• Licensed MD or PhD with a background in endocrinology or a related field.
• At least 2 years of clinical trial experience as a medical monitoring associate or in an equivalent relevant role.
• Demonstrated experience supporting clinical trial strategy and FDA submission activities.
• Experience with protocol development and medical writing for protocols and clinical study reports.
• Strong understanding of FDA interactions and clinical regulatory processes.
• Endocrinology expertise required; pediatrics and metabolic trial experience are preferred.
• Strong written and verbal communication skills, with the ability to collaborate effectively across clinical and medical teams.
• Ability to work independently, manage priorities, and provide reliable support in a project-based environment.
• Working knowledge of Excel and Clinical Trial Management Systems (CTMS).