Assisting Clinical Research Associates (CRAs) with routine tasks, document submission, safety reporting, remote monitoring, and regulatory document collection. Requires fluency in English and local language, higher education, and knowledge of clinical trial regulations.
📌 Contractor Cra_spain (Madrid)
🏢 Cromos Pharma
📍 Madrid
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Muestra tus habilidades a la empresa, rellenar el formulario y deja un toque personal en la carta, ayudará el reclutador en la elección del candidato.