McLaren Health Care Clinical Research Coord II in Detroit, Michigan
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.
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
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: 19006812