OPIS is seeking a Clinical Research Associate to manage and monitor trials ensuring compliance with study protocols, ICH-GCP, and regulatory requirements.
La información a continuación detalla los requisitos del puesto, la experiencia esperada del candidato y las cualificaciones correspondientes.
You will oversee site initiation, monitoring, and close-out while safeguarding data quality and patient safety.
The role requires a degree in a scientific field and at least 2 years of CRA experience, preferably in oncology and early-phase studies. xqbhyrx
Excellent English and MS Office skills are essential.
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📌 Clinical Research Associate: Trials Monitoring & Compliance (España)
🏢 Opis
📍 España