Senior Clinical Monitoring Lead — Travel-Heavy CRA II
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Fortrea is seeking a Lead CRA based in Belgium to manage site monitoring activities for clinical studies in line with ICH GCP, SOPs and sponsor requirements. You will ensure subject protection, data integrity, regulatory document completeness, and audit readiness across sites.
The role involves 60% travel to study sites, coordinating with the study team, preparing monitoring plans, and leading on-site visits, training staff, and ensuring timely trips and reports.