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    Clinical Research Technician/Assistant - Ann Arbor, United States - University Of Michigan

    University Of Michigan
    University Of Michigan Ann Arbor, United States

    1 week ago

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    Description
    Summary

    This position may independently provide study coordination for simple and moderately complex clinical research studies.

    As a member of a coordination team, this position may help support a portfolio of projects with varying levels of complexity.

    Responsibilities*This position may independently provide study coordination for simple and moderately complex clinical research studies.

    As a member of a coordination team, this position may help support a portfolio of projects with varying levels of complexity.

    Mastery of all job duties from previous job description is required.

    Experience as part of a team with all 8 competency domains is expected:


    • Scientific Concepts and Research Design
    • Ethical Participant Safety Considerations
    • Investigational Products Development and Regulation
    • Clinical Study Operations (GCPs)
    • Study and Site Management
    • Data Management and Informatics
    • Leadership and Professionalism
    • Communication and Teamwork

    Specific competencies include:

    • Conduct/schedule study participant visits
    • Identify eligible study subjects
    • Obtain informed consents from study subjects
    • Collect and process specimens collected from study subjects
    • Assist with regulatory activities
    • Coordinate, facilitate and conduct correct timing of study visits and procedures with patients and staff
    • Enter participants research data into an electronic data entry system
    The above statements are intended to describe the general nature and level of work to be performed and are not an exhaustive list of all associated responsibilities

    Required Qualifications*Clinical Research Technician


    • Associate degree in Health Science or an equivalent combination of related education and experience is necessary.
    • At least one of the following:
    • Minimum 1 year of directly related experience in clinical research and clinical trials is necessary. (Please review SoCRA?s Definition of a Clinical Research Professional
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