07 ott - Milano
Iqvia
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 xysqume solid GCP/ICH knowledge, 3+ years on-site monitoring experience, and strong communication skills in English; proficiency
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