Clinical Research Coordinator II

Job Summary : Provide study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO). Manage independent assignment, providing excellent customer support and guidance in the clinical trials arena. Responsibilities Assure all study requirements are met and documented and meet both internal and external regulations in accordance with protocol guidelines. Maintain logs, including tracker submissions and update the CTO Oncore database in a timely manner according to CTO SOPs. Design systems for coordinating, compiling and submission of data; design workflow processes and participate in quality assurance measures; coordinate site visits. Manage all patient and/or protocol data as assigned and respond to queries in a timely fashion. Schedule and participate in monitoring visits and participate in multidisciplinary team program meetings as required. Coordinates clinial trials onboarding for physicians, non-physicians providers, clinical staff, and clinical trials office personnel. Maintains the National Cancer Institute's (NCI) registrations to support clinical trials participation and ongoing compliance. Provides operational and administrative support of KCI CTO electronic clinical research system. Bachelor’s degree required or equivalent combination of education and experience. Medical and/or science experience/education preferred. Clinical research certification preferred. Equal Opportunity Employer of Minorities/Females/Disabled/Veterans Additional Information Schedule: Full-time Daily Work Times: 8am-4:30pm Hours Per Pay Period: 80 On Call: No Weekends: No #J-18808-Ljbffr McLaren Health Care