Clinical Trial Coordinator FSP

The Clinical Trial Coordinator – Project Specialist will partner with the Study Manager on end-to-end operational study delivery, focusing on internal systems, databases, and project plans. They will collaborate cross-functionally with internal and external partners on clinical study management activities, ensuring compliance with regulations and procedures. Responsibilities include supervising study conduct, reviewing key clinical documents, developing study plans, facilitating interactions with partners, overseeing vendors and CROs, managing country-specific activities, coordinating study team communications, leading the delivery of clinical supplies, ensuring data oversight and eTMF completeness for inspection readiness, and managing study budgets and change orders. The role also involves contributing to continuous improvement initiatives and operational efficiency.