FSP - Clinical Trial Coordinator

Coordinate and oversee functions on assigned trial activities. Perform internal and investigator file reviews, ensuring tasks are completed on time and within budget. Support the maintenance of study-specific documentation and provide system support for tools like GoBalto and eTMF. Assist with administrative tasks including document processing and scheduling meetings.

High school diploma or equivalent required; Bachelor's degree preferred. At least 4 years of relevant experience in clinical trials. Strong organizational skills and ability to analyze project-specific data. Proficiency in MS Office and clinical trial database systems.