Teams at Fortrea

Perform site monitoring and management for clinical studies including initiation, routine monitoring, closeout, CRF/source data review, SAE tracking, regulatory submissions, vendor liaison, CTMS and study file maintenance, travel for site visits, and support training and local project coordination as assigned.

Provide administrative and systems support for clinical trial teams: maintain TMF and project documentation, track study activities and supplies, prepare site materials, take minutes, coordinate shipments and vendors, generate reports, assist with TMF QC and CAPA tracking, and communicate with sponsors, sites and internal teams.

Perform site monitoring and management for clinical trials per SOPs, ICH GCP and sponsor requirements. Conduct initiation, routine, and close-out visits; verify informed consent and source data; manage regulatory documents, IP accountability, SAE follow-up, eCRF review, and eTMF/CTMS maintenance. Prepare reports, train site staff, and travel frequently to sites.