17 oct
|
Opis
|
Barcelona
OPIS is hiring a Clinical Research Associate to manage and monitor multi-country trials, ensuring adherence to ICH-GCP and regulatory standards. You will oversee site selection, initiation, monitoring, and close-out activities, while safeguarding data quality and patient safety.
The role reports to the Clinical Project Manager and involves collaboration with sponsors, sites, and project teams. Requires a scientific degree and 2+ years’ CRA experience, with strong English and MS Office skills.
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📌 Clinical Research Associate: Monitor Trials & Data Quality (Barcelona)
🏢 Opis
📍 Barcelona