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McLaren Health Care Clinical Research Coord II in Detroit, Michigan

Description

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.

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

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

Schedule Full-time

Req ID: 19006812

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