Teams at Fortrea

Lead local laboratory data management across clinical studies, overseeing data acquisition, transfers, reconciliation, quality checks, vendor and site interactions, system configuration, and query resolution. Collaborate with sponsors and cross-functional global teams throughout study start-up, maintenance, and database lock. Ensure compliance with protocols, GCP, ICH guidelines, FDA regulations, SOPs, and audit-readiness requirements while supporting process improvements, risk management, and local lab standards.

Forecast investigator grants and clinical trial site payments across global studies. Translate protocol and operational assumptions into payment and cash-flow forecasts, reconcile forecasts with actuals, analyze payment drivers and variances, support accruals and month-end close, build executive dashboards, conduct scenario planning, maintain audit-ready documentation, and improve forecasting processes and technology in partnership with Clinical Operations, Finance, Contracts, and CROs.

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.