Icon Clinical PLC is seeking a Clinical Research Associate II in Barcelona to oversee site qualification, initiation, monitoring, and close-out visits for clinical trials. You will ensure protocol compliance, data integrity, and patient safety while collaborating with investigators and site staff to facilitate study conduct. The role requires 2+ years in CRA, knowledge of ICH-GCP, and a strong ability to work independently in a fast-paced environment.
📌 Clinical Research Associate II: Global Trials (Barcelona)
🏢 Icon Clinical
📍 Barcelona
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