Sponsor-Focused Clinical Research Associate
IQVIA
IQVIA is seeking a Clinical Site Monitor in the United States to perform site monitoring visits, ensure protocol compliance and data reporting, and support study management. You will work with sites to drive recruitment, provide protocol training, and track regulatory milestones. The role requires at least 2 years of on-site monitoring experience, strong knowledge of GCP and ICH guidelines, and solid English communication, organizational, and time/financial management skills. #J-18808-Ljbffr IQVIA
Vacancy posted 3 days ago
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