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.

Lead end-to-end operational strategy and delivery for Phase I clinical trials. Manage scope, timelines, risk, budget, and client relationships across global, matrixed teams. Mentor staff, oversee financials and KPIs, ensure regulatory and quality compliance (ICH/GCP), and drive issue escalation and resource planning.

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.