Teams at Fortrea

Conducts oncology clinical trial site monitoring, including routine, initiation, and close-out visits; verifies informed consent, protocol compliance, patient safety, and data integrity; manages study files, registries, vendors, and serious adverse event reporting; performs CRF review and query resolution; supports feasibility activities, employee training, and local project coordination. Requires frequent overnight travel across Southern California and occasional domestic or international travel.

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.