Clinical Research Associate - Site Monitoring & Coordination
IQVIA
IQVIA in the United States seeks a site monitor based in California to ensure that sites conduct studies and report data per protocol, regulations, and sponsor requirements. You will perform site visits, support recruitment planning, train site staff, and track regulatory submissions, CRF completion, and data queries, while maintaining TMF/ISF records. The role emphasizes strong communication, organization, and time/financial management, with on-site collaboration across study teams. #J-18808-Ljbffr IQVIA
Vacancy posted 4 days ago
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