FSP Clinical Trial Coordinator

The Clinical Trial Coordinator will partner with the Study Manager on end-to-end operational study delivery, focusing on setting up and maintaining internal systems and project plans. They will work cross-functionally with internal and external partners on clinical study management activities, monitor study conduct, identify and resolve risks, and review key clinical documents. Responsibilities include leading the development of study plans, facilitating interactions with partners, managing vendors and CROs, overseeing country-specific activities, coordinating study-related communications, overseeing the delivery of clinical supplies, ensuring data oversight and eTMF completeness for inspection readiness, and managing budget oversight including task/change orders and expenses.