CRA 1, IQVIA Biotech

Conduct site selection, initiation, routine, and close-out monitoring visits to evaluate site practices, verify regulatory compliance, and ensure protocol adherence. Review essential documents, assess data entry and query resolution, and maintain the Trial Master File and Investigator Site File. Provide protocol training, address site challenges, and support recruitment planning to meet enrollment targets. Prepare detailed monitoring visit reports and follow-up letters to ensure audit readiness. Manage multiple tasks independently while collaborating with internal project teams. Requires 6 months of on-site monitoring experience in oncology solid tumor, with a base pay range of $71,900 to $119,900 annually.