Jobs at Fortrea

Lead and coordinate study start-up/site activation across countries, guide site activation specialists, develop country-specific ICFs, use data/forecasting to drive timelines, mentor team members, identify process improvements, and escalate/resolves start-up delays to achieve Ready-to-Enroll status.

Lead site budget and contract activities across assigned UK/ROI countries, negotiate Clinical Trial Agreements and site budgets, escalate and resolve complex issues, monitor timelines, support country-level budget setup, use market data to inform decisions, drive process improvements, and ensure sites are contractually and financially ready for patient enrollment.

Conduct and oversee site monitoring visits for Phase II/III interventional trials to ensure protocol, GCP, regulatory, and SOP compliance. Manage site initiation, routine monitoring, and closeout; ensure patient safety and data integrity; report and follow up on SAEs; support site feasibility and investigator engagement; maintain documentation and communicate with sites and project teams; travel within Ireland as needed.

Coordinate site start-up activities, collect and submit regulatory documents (EC/IRB/RA), ensure ICH/GCP compliance, track timelines, maintain audit-ready documentation, support contracts/budgets, liaise with stakeholders, and mentor new or less-experienced colleagues to enable efficient site activation.

Negotiate, prepare, and manage site agreements, confidentiality agreements, and indemnification letters for clinical trials; ensure regulatory and SOP compliance; track contract status; collaborate with study teams, legal, and project management; maintain contract files; escalate issues and support process improvements.