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    Clinical Research Coordinator - Albuquerque, United States - Medix™

    Medix™
    Medix™ Albuquerque, United States

    5 days ago

    Default job background
    Description

    Looking for an entry level Clinical Research Coordinator and an experienced Clinical Research Coordinator to join our team

    Entry Level Clinical Research Coordinator - 6 months - 1 year required

    • Must be comfortable with oncology studies

    Experience Level Clinical Research Coordinator - 2 years - 3 years required

    • Must have experience with oncology studies
    • With assistance, prepares and processes new IRB research proposals, amendments,

    continuing review applications and adverse event reports according to institutional and

    departmental policies and procedures and federal regulations

    • Prepares and maintains documents required to be maintained and available internally and

    for regulatory authorities and/or the sponsor prior to, during and after the conduct of a

    clinical/translational trial. Participates in periodic site visits from sponsor, regulatory

    authorities and others to review research, source documentation and research procedures

    • Procures equipment and supplies needed to fulfill project requirements
    • Records data from source documentation and/or participant interaction onto case report

    forms (either paper or electronic) with awareness and attention to the requirements for

    accuracy, completeness and timeliness. Attends to query resolution in a timely manner.

    • Assures research information is collected and stored in a manner that is compliant with

    regulations/policies and good clinical practice

    • Performs packaging and ships study specimens (blood, urine, etc.) to the sponsor or

    laboratory in accordance with sponsor and shipping guidelines and regulations, maintaining

    appropriate documentation

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