Teams at Fortrea

Support acquisition, review, and integration of external clinical trial data; perform data quality checks; coordinate with internal teams and vendors; contribute to study deliverables and timelines across multiple studies and therapeutic areas.

Lead programming activities, mentor programmers, develop and maintain SAS programs for SDTM and ADaM datasets, and ensure quality control.

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.