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 studyrequirements are met and documented and meet both internal and externalregulations in accordance with protocol guidelines. + Maintain logs,including tracker submissions and update the CTO Oncore database in atimely manner according to CTO SOPs. + Design systems forcoordinating, compiling and submission of data; design workflow processesand participate in quality assurance measures; coordinate site visits. + Manage all patientand/or protocol data as assigned and respond to queries in a timelyfashion. + Schedule andparticipate in monitoring visits and participate in multidisciplinary teamprogram 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