Jobs at Fortrea

Lead and own operational strategy for oncology clinical trials, managing scope, timeline, budget, risk, and quality. Build and mentor cross-functional global teams, drive client relationships, ensure regulatory and SOP compliance, forecast finances, manage resources and change control, and deliver presentations for business needs.

Lead end-to-end ophthalmology clinical trials, owning strategy, timelines, budget, risk, and quality. Build and mentor cross-functional teams, manage client relationships, forecast revenue, and ensure compliance with ICH/GCP and company SOPs while driving patient-centric, cost-effective delivery.

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.