McLaren Health Care Clinical Research Coord I in Detroit, Michigan
Provide study coordinator/data
management/regulatory specialist support to the Clinical Trials Office (CTO).
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
Job: Non-Health Professional
Primary Location: Michigan-Detroit-Mid Med Building
Organization KCI30-Karmanos Cancer Institute
Employee Status Regular
Shift Day Job
Job Type Standard
Req ID: 20010180