• Clinical Research Coordinator II - McLaren Careers

    McLaren Health Care (Detroit, MI)


    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