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    Clinical Research Coordinator, CHERISH - New Orleans, United States - Tulane University

    Tulane University
    Tulane University New Orleans, United States

    1 week ago

    Default job background
    Description

    The primary responsibility of the Clinical Research Coordinator is to coordinate and conduct the day-to-day operation of clinical studies and clinical trials related to cardiovascular disease.

    The Clinical Research Coordinator assists the investigator team to develop study protocols and manuals of procedures.

    The Clinical Research Coordinator screens, enrolls and follows study participants, conducts data collection and entry, and performs noninvasive cardiovascular tests according to study protocols.

    The Clinical Research Coordinator is also responsible for keeping all data and source documentation, adverse event reporting, and IRB regulatory files.


    • Must be able to interact well with participants and the general public
    • Ability to acquire and maintain all required CITI training certificates
    • Ability to acquire and maintain credentialing at all required institutions
    • Willing to travel to conduct church visits
    o This role involves travel most days to churches in the greater New Orleans area

    The education required for each level is listed below:

    Clinical Research Coordinator I (Pay Grade 23)


    • Bachelor's Degree or RN with current state licensure at the time of hire
    OR


    • LPN with current state licensure at the time of hire and three (3) years of related work experience
    Clinical Research Coordinator II (Pay Grade 24)


    • Bachelor's Degree or RN with current state licensure at the time of hire
    and one (1) year of related work experience

    OR


    • LPN with current state licensure at the time of hire and four (4) years of related work experience
    OR


    • Master's Degree in a related field
    Clinical Research Coordinator III (Pay Grade 25)


    • Bachelor's Degree or RN with current state licensure at the time of hire
    and two (2) years of related work experience

    OR


    • LPN with current state licensure at the time of hire and five (5) years of related work experience
    OR


    • Master's Degree and one (1) year of related work experience
    Level I


    • Expressed interest in Clinical Research
    • Motivated to learn about Clinical Research and associated regulations
    Level II


    • Knowledge of IRB submission process and requirements
    • Knowledge of good clinical practices as set forth by federal regulations
    Level III


    • Certification as a Certified Clinical Research Coordinator (CCRC through the Association of Clinical Research Professionals or ACRP) OR Certified Clinical Research Professional (CCRP through the Society of Clinical Research Associates or SoCRA)
    • Supervisory experience
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