ICON plc is a world-leading healthcare intelligence and clinical research organization committed to advancing treatments and patient care. As a Clinical Research Associate at ICON, you will design and analyse trials, monitor sites, and ensure data integrity while prioritizing patient safety.
Key responsibilities include site visits, data review, and collaboration with investigators to ensure compliant, high-quality study conduct. Travel up to ~60% is expected in this fast-paced, impactful role.
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📌 Travel‑Ready Clinical Research Associate: Site Monitoring (Milano)
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📍 Milano