Teams at Fortrea

Conduct clinical trial site monitoring, including pre-study, initiation, routine monitoring, and close-out visits. Ensure protocol compliance, informed consent, participant protection, data integrity, SAE reporting, CRF review, query resolution, registry management, and study file maintenance. Liaise with vendors, support feasibility activities, train new employees, and coordinate designated clinical projects. The role requires frequent domestic and occasional international travel.

Lead and deliver global oncology clinical projects by managing scope, schedule, budget, quality, risks, and stakeholder communications. Oversee cross-functional teams, ensure regulatory and GCP compliance, mentor staff, support business development, and maintain project KPIs and resource planning.

The Sr. CRA 2 will monitor clinical trial sites, manage study compliance, ensure data integrity, and oversee patient safety in oncology studies, requiring strong clinical judgment and teamwork.