OPIS is seeking a Clinical Research Associate to manage and monitor multi-country trials in compliance with study protocols, ICH-GCP, and applicable regulations. You will oversee site selection, initiation, monitoring, and close-out activities while ensuring data quality and patient safety, reporting to the Clinical Project Manager.The role requires a scientific degree, at least two years in CRA or trial monitoring (oncology/phase 1 preferred), and strong knowledge of ICH-GCP and ISO14155.
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📌 Clinical Research Associate: Monitoring & Compliance (Madrid)
🏢 Opis
📍 Madrid