Clinical Trial Site Monitor & Study Quality Lead
IQVIA
IQVIA in Overland Park, KS seeks a Clinical Research Associate to monitor sites, ensure study data collection complies with the protocol, GCP and ICH guidelines, and sponsor requirements. You will lead site visits, recruit and train staff, manage regulatory submissions and data queries, maintain TMF/ISF filings, and collaborate with the study team to support project goals and timelines. #J-18808-Ljbffr IQVIA
Vacancy posted 5 days ago
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