Senior CRA: Site Monitoring & Study Oversight

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/8daksc

IQVIA LLC is seeking a Clinical Research Associate responsible for site monitoring and study management to ensure protocol adherence, data quality, and regulatory compliance across assigned sites in Italy.
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You will conduct monitoring visits, manage recruitment plans, and coordinate with site staff, with IQVIA's global leadership in clinical research services.

The role requires solid GCP/ICH xysqume knowledge, 3+ years on-site monitoring experience, and strong communication skills in English; proficiency

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Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/8daksc