Teams at Fortrea

Lead and develop Clinical Data Management teams, oversee resource planning, quality, productivity, and operational delivery for global clinical trials. Partner with cross-functional stakeholders, drive process improvements, support recruitment and training, ensure regulatory and SOP compliance, and contribute to business development and client-facing activities.

Lead and oversee statistical programming for clinical studies: develop and QC SAS programs to produce SDTM/ADaM datasets and TFLs, create Define-XML/ARM/annotated CRFs, review SAP/TFL shells, mentor junior programmers, interact with clients and QA, and improve programming processes.

Lead and oversee centralized and risk-based monitoring activities across global clinical studies. Identify risks, trends, and safety concerns, drive risk assessments, monitoring plans, analytics, dashboards, and data-driven strategies. Partner with study teams and sponsors, ensure ICH-GCP and regulatory compliance, and support continuous process improvements and sponsor-facing activities.