Senior CRA II – Travel-Heavy Clinical Monitoring Lead
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Fortrea is seeking a Lead Clinical Research Associate to manage site monitoring for multicenter trials in Belgium. The role emphasizes adherence to ICH GCP, regulatory requirements, and Fortrea SOPs, with extensive travel and coordination of site activities.
You will verify informed consent, monitor data integrity, and ensure regulatory documents are complete. The position requires strong planning, organization, and independent work capabilities in a matrix environment.