Fortrea in Madrid is seeking an experienced CRA/clinical monitor responsible for site monitoring and site management of clinical studies in accordance with SOPs and regulatory guidelines. You will ensure project plans are implemented, coordinates with vendors, and oversee data integrity and site readiness.
The role requires strong regulatory knowledge, English proficiency, and the ability to work in a matrix environment, with travel as needed to sites.
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📌 Clinical Research Associate I — Site Monitoring & Trial Support (Madrid)
🏢 Fortrea
📍 Madrid
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