OPIS s.r.l. is seeking a Clinical Research Associate to monitor and manage multi-country clinical trials, ensuring compliance with study protocols, ICH-GCP, and regulatory requirements.
This role emphasizes site initiation, monitoring visits, data quality, and patient safety, reporting to the Clinical Project Manager. The successful candidate will have a scientific degree, at least two years of CRA or trial monitoring experience (oncology and phase 1 studies preferred), strong English, and
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📌 Clinical research associate: oncology trials specialist (España)
🏢 Opis S. R. L.
📍 España
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