FSP Clinical Trial Coordinator II

Coordinate and facilitate project activities for assigned trials. Perform internal and investigator file reviews, ensuring tasks are completed on time and within budget. Support maintenance of study documentation and provide system support for tools like GoBalto and eTMF. Analyze study metrics and assist with site documentation clarification.

High school diploma or equivalent required; Bachelor's degree preferred. At least 4 years of relevant experience in clinical trials. Strong organizational skills, attention to detail, and proficiency in MS Office. Excellent English language skills and ability to work independently or in a team.