FSP Bench Clinical Trial Coordinator

Assists in coordination and administration of clinical studies from start-up to execution and close-out. Collects, prepares, reviews, and tracks documents for application processes, ensuring timely submissions to EC/IRB and regulatory authorities. Manages local eTMF and ISF, ensuring essential documents are uploaded for inspection readiness. Coordinates administrative tasks during study processes and contributes to the preparation of internal and external meetings.

High/Secondary school diploma or equivalent; Bachelor's degree preferred. Previous experience of 2+ years in a relevant role. Strong organizational skills, attention to detail, and ability to analyze project-specific data. Proficient in MS Office and clinical trial database systems.