FSP Bench Clinical Trial Coordinator

Assists in coordination and administration of clinical studies from start-up to execution and close-out. Collects and tracks documents for application processes, ensuring timely submissions to 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. Good English language skills and proficiency in local language as needed. Strong computer skills, particularly in MS Office and clinical trial database systems.