Oncology CRA II: Site Monitoring & Compliance Pro
ICON Clinical Research
ICON Clinical Research in Chicago is seeking a Clinical Research Associate to serve as the primary contact between investigational sites and the sponsor. Responsibilities include conducting site visits, ensuring compliance with regulations, and monitoring patient safety. The ideal candidate will have a bachelor's degree, 2+ years of experience in clinical research, and familiarity with oncology trials. ICON offers a competitive salary along with various benefits focused on well-being and work-life balance. #J-18808-Ljbffr ICON Clinical Research
Vacancy posted 18 hours ago
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