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 the local eTMF and ISF, ensuring essential documents are uploaded timely for inspection readiness.

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.