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    Clinical Research Coordinator - Kansas City, United States - Medix™

    Medix™
    Medix™ Kansas City, United States

    3 weeks ago

    Default job background
    Engineering / Architecture
    Description

    Clinical Research Coordinator - Kansas City, MO

    Hours: Monday - Friday, 8am-5pm

    Pay: $25 - $30/hour

    Location: Kansas City, Missouri 64151

    We are seeking an experienced Clinical Research Coordinator to join one of America's largest rheumatology clinics and research facilities.

    Responsibilities:

    • Enroll patients into clinical research studies following established protocols and procedures.
    • Obtain informed consent from study participants, ensuring they understand the purpose, procedures, risks, and benefits of the study.
    • Coordinate and conduct patient visits according to the study schedule.
    • Monitor and document patient progress and report any adverse events or protocol deviations to the principal investigator.
    • Actively recruit potential study participants by foPerform venipuncture to collect blood samples for clinical research and diagnostic purposes, ensuring patient comfort and adherence to protocol.
    • Perform venipuncture to collect blood samples for clinical research and diagnostic purposes, ensuring patient comfort and adherence to protocol.
    • Conduct and process laboratory tests, ensuring accurate and timely collection of specimens for research studies.
    • Administer electrocardiograms (EKGs) to monitor and record participants' cardiac activity as required by study protocols.
    • Administer medications, both oral and injectable, to study participants according to prescribed protocols and safety guidelines.
    • Collaborate with nursing staff to assist with the preparation and administration of intravenous infusions, ensuring proper technique and participant safety.
    • Maintain controlled environmental conditions for study supplies and medications, ensuring adherence to specified temperature and storage requirements.
    • Manage inventory of study-related materials, including tracking, ordering, and replenishing supplies as needed to support ongoing research activities.

    Qualifications:

    • 2 years experience as a CRC
    • Strong patient facing and a patient recruitment background

    Preferred Qualifications:

    • Background in Oncology or Rheumatology
    • Bachelors degree
    • ACRP or SOCRA certified
    • Phase II-III pharma experience
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