Description Become part of an inclusive organization with over 40,000 teammates, whose mission is to improve the health and well-being of the unique communities we serve.Summary:The primary purpose of this position is to ensure our site?s compliance in conducting clinical research in all our facilities.Responsibilities:1.Independently administer regulatory compliance for assigned studies, applying full knowledge of Good Clinical Practice (GCP) and the federal regulations governing clinical research in the United States.2.Take responsibility for IRB submissions and modifications (accurate & timely preparation for initial reviews, amendments, annual renewals and ad hoc submissions).3.Provide appropriate training and complia