Scheduled Hours40Position SummaryManage all regulatory-related activities for a large portfolio of human clinical trials. Position oversees and coordinates administrative aspects of complex clinical research studies. Serve as a resource to provide comprehensive information to clinical research staff by promoting a smooth operation of clinical research. Responsible for preparation of budgetary reports and ensures billing and regulatory compliance standards are maintained. May supervise clinical research staff.Job DescriptionPrimary Duties and ResponsibilitiesResponsible for all IRB submissions and updates, creating consent forms, coordinating with Clinical Research Organization and Study Sponsor
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