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    Clinical Research Coordinator - Chicago, United States - Medix

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    CLINICAL RESEARCH COORDINATOR OPPORTUNITY IN CHICAGO, IL
    MUST HAVE CLINICAL RESEARCH EXPERIENCE Clinical Research Coordinator Job Description Coordinates all aspects of the study including recruitment, consent, screening, scheduling, tracking and provides study updates to study participants throughout the conduct of the studyMay collect and enter data into study case report forms and/or electronic data capture system and respond to queries in a timely manner.

    Submits or partners with a regulatory coordinator to submit study related documents, study protocols and study protocol amendments to the IRB per policy and procedureEnsures procedural documentation is accurate, complete, and in compliance with institutional, local, state and federal guidelines and regulations related to clinical research.

    May collect, process and ship potentially biohazardous specimensMay administer more complex structured tests and questionnaires according to research study protocols.

    May utilize study-related technology and equipment as part of assessment procedures.
    Provide ongoing study status updates, responds to questions and may create summary report(s) for distribution to PI, Administrator, Office of Research Affairs, Sponsor and Compliance throughout the conduct of the studyOrganize and participate in auditing and monitoring visitsRequirements: Bachelor's/Associate's degree or equivalent experience1-2+ years of experience in

    Clinical Research Details:
    Location: Chicago, IL Pay: $55K-$75K (Dependent on background and years of experience)

    Hours:
    Monday - Friday; Normal Business Hours; Onsite 5 Days a

    Week Duration:
    ~6 month (1,040 Hours) contracted probationary period into direct hire / permanent position


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