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Clinical Research Associate — Site Monitoring & Recruitment

IQVIA

IQVIA is seeking an on-site Clinical Research Site Monitor in California to ensure sites conduct studies per protocol, regulations, and sponsor requirements. You will monitor visits, manage recruitment plans, and train site staff to uphold data quality and regulatory compliance. The role requires at least 2 years of monitoring experience, knowledge of GCP/ICH, and strong communication and organizational skills. Travel and collaboration with study teams are common in this position. #J-18808-Ljbffr IQVIA

Vacancy posted 1 day ago
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