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. **This position is onsite in Detroit, Michigan.** **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. * 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