• Clinical Research Coordinator II - McLaren Careers

    McLaren Health Care (Detroit, MI)


    Job Summary:

    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 study requirements are met and documented and meet both internal and external regulations in accordance with protocol guidelines.

    + Maintain logs, including tracker submissions and update the CTO Oncore database in a timely manner according to CTO SOPs.

    + Design systems for coordinating, compiling and submission of data; design workflow processes and participate in quality assurance measures; coordinate site visits.

    + Manage all patient and/or protocol data as assigned and respond to queries in a timely fashion.

    + Schedule and participate in monitoring visits and participate in multidisciplinary team program meetings as required.

    Qualifications:

    + 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