Descrizione dell'offerta
ARTO is seeking an experienced Italian-based Senior CRA for a freelance opportunity to support clinical study start-up activities. The role centers on regulatory submission support, IRB/document preparation and tracking, and site activation with essential documents.
The ideal candidate has senior CRA experience in the US and direct experience with regulatory submissions and IRB documentation, plus strong knowledge of FDA regulations, ICH-GCP, and US site requirements.
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Candidatura e Ritorno (in fondo)
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