Clinical Research Assistant — Study Coordination & Data Entry
Paycom
Paycom in Wisconsin seeks a Clinical Research Coordinator to support study protocols, obtain consent, and ensure regulatory compliance. You will work closely with study teams to screen candidates, document procedures, and maintain source data in EDC and EMR systems. Responsibilities include coordinating visits, collecting specimens, performing measurements, managing inventory, and communicating with sponsors, IRB, and investigators. Strong knowledge of HIPAA, GCP, and FDA regulations is required. #J-18808-Ljbffr Paycom
Vacancy posted 2 days ago
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