Teams at Fortrea

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.