Responsibilities

The Clinical Trial Coordinator will provide administrative and technical support to the project team, coordinating assigned trial activities and ensuring adherence to timelines and quality standards. They will conduct file reviews, support site activation activities, train new staff, and maintain study-specific documentation, including system support and document tracking. Additionally, the role involves assisting with regulatory document reviews, transmitting documents to clients, analyzing study metrics, and coordinating the preparation of Investigator Site Files and Pharmacy binders, as well as supporting RBM activities and translation materials.