Clinical Trial Coordinator FSP

The Clinical Trial Coordinator – Project Specialist will partner with the Study Manager or Study Delivery Lead on end-to-end operational study delivery activities, focusing on setting up and maintaining internal systems, databases, and project plans. They will work cross-functionally with internal and external partners on clinical study management activities, supervise study conduct and progress, and identify/resolve risks. Responsibilities include reviewing key clinical documents, developing study plans, facilitating interactions with internal and external partners, managing vendors and CROs, overseeing country-specific activities, coordinating study-related communications and meetings, overseeing the delivery of clinical supplies and investigational products, ensuring data oversight and eTMF completeness for inspection readiness, and managing study budgets including Task/Change Orders and expenses. The role also involves contributing to squads as per STOM requirements.