FSP Principal CTC

Coordinate and facilitate project activities as a study lead, ensuring tasks are scheduled and fulfilled according to project needs. Perform internal and investigator file reviews, document findings, and maintain study-specific documentation. Support project teams in audit readiness and assist with the negotiation and finalization of site agreements and budgets.

High school diploma or equivalent required; Bachelor's degree preferred. At least 6 years of relevant experience in clinical trial coordination. Knowledge of regulatory guidelines and experience with project management tools is essential.