Provide study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO). **Responsibilities:** + Assure all studyrequirements are 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. + Respond to queriesin a timely fashion. + Schedule andparticipate in monitoring visits and participate in multidisciplinary teamprogram meetings as required. + Assistmultidisciplinary team in research activities. * Bachelor’s degree required or equivalent combination of education and experience. * Medical and/or science experience/education preferred. * Proficient with the Microsoft suite including Excel and Power point. * Demonstrated attention to detail. Equal Opportunity Employer of Minorities/Females/Disabled/Veterans