Senior Clinical Research Associate | Site Monitoring
$74.5kIQVIA
IQVIA in the United States seeks a diligent Clinical Trial Site Monitor based in Kansas. You will perform site monitoring visits, manage recruitment plans, and ensure GCP/ICH compliance across assigned sites. You will train site staff, maintain regular communication, track submissions and data queries, and help keep TMF and ISF up to date. Strong English, organization, and collaboration are essential. This role offers exposure to multiple studies with a base pay range described as $74,500 to #J-18808-Ljbffr IQVIA
Vacancy posted 3 days ago
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