Jobs at Fortrea

Lead on-site clinical monitoring and site management for oncology studies, ensuring protocol compliance, informed consent, data integrity (CRF review/query resolution), SAE reporting, registry management, initiation and close-out visits, vendor liaison, training/co-monitoring, and acting as local project coordinator. Significant travel to study sites required.

Lead and conduct on-site clinical trial monitoring for radiopharmaceutical therapy studies, ensuring protocol adherence, patient safety, informed consent, CRF/data integrity, SAE reporting, site management, feasibility, and training. Act as local project coordinator and client contact as assigned, perform monitoring visits, close-outs, and data query resolution using sponsor/CRO data systems.

Perform on-site and remote clinical site monitoring, ensure regulatory compliance and informed consent, review CRFs/EDC data, manage registries, report and follow up SAEs, support site initiation and close-out, train/co-monitor staff, and coordinate local project activities with frequent travel.

Lead site monitoring activities for in vitro diagnostic clinical studies including initiation, routine and close-out visits; ensure regulatory compliance, informed consent, data integrity, SAE reporting, CRF review, vendor liaison, registry management, and occasional project coordination. Frequent travel required.

Lead and perform on-site clinical monitoring for oncology CAR-T trials including site initiation, routine and close-out visits, CRF review, SAE reporting, source document verification, vendor liaison, feasibility, registry management, and training/co-monitoring responsibilities.

The role involves monitoring clinical trial sites, ensuring protocol adherence, reporting serious adverse events, and training new staff, with 5+ years' experience required.

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.

The Sr. CRA 2 will monitor clinical trials, manage study sites, ensure regulatory compliance, and assist with training and data integrity verification.

Responsible for monitoring clinical trials, ensuring compliance with protocols, data integrity, site management, and training new employees, with significant oncology experience required.