06 ott - Firenze
Altro
Trial Form Support is seeking a remote Clinical Trial Monitor specializing in oncology to oversee site monitoring, data integrity, and regulatory compliance across global sites. You will ensure patient safety, validate informed consent, and manage trial documentation in line with GCP/ICH standards.
In this home-based role, you will coordinate monitoring activities, support audits, and travel 60-80% domestically and abroad, contributing to high-quality study conduct and meaningful patient
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