Teams at Fortrea

Conducts Phase I clinical trial site monitoring and management, including pre-study, initiation, routine monitoring, and close-out visits. Ensures protocol compliance, informed consent, participant safety, data integrity, and regulatory adherence. Performs CRF review, query resolution, registry management, feasibility work, and Serious Adverse Event reporting. Coordinates assigned clinical projects, liaises with vendors and clients, supports study staff training, and travels approximately 40–50% overnight to domestic and occasional international sites.

Conducts clinical trial site monitoring and management, including initiation, routine and close-out visits; verifies informed consent, protocol compliance, patient safety, and data integrity; manages CRFs, queries, serious adverse event reporting, registries, vendors, and study documentation. May train employees and coordinate local clinical projects. Requires 4+ years of clinical monitoring experience, an allied health degree or certification, and more than 50% overnight travel.

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.