05 ott - Padova
Altro
Trial Form Support seeks a capable Clinical Trial Monitor to oversee oncology trials across sites, ensuring patient safety, data integrity, and regulatory compliance from a home-based setting. You will coordinate monitoring activities, manage documentation, and support audits to enable successful study execution.
The role requires at least 3 years in monitoring oncology trials (including early-phase), strong GCP/ICH knowledge, and fluency in English.
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