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    Clinical Research Coordinator, MH-CIP - 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 maternal health and diabetes.

    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 patients and the general public
    • Ability to acquire and maintain all required CITI training certificates
    • Ability to acquire and maintain credentialing at all required institutions
    The education required for each level is listed below:

    Clinical Research Coordinator I (Pay Grade 23)


    • Licensed Practical Nurse with current state licensure at the time of hire and 3 years of related work experience
    OR


    • Bachelor's Degree or Registered Nurse with current state licensure at the time of hire
    Clinical Research Coordinator II (Pay Grade 24)


    • Licensed Practical Nurse with current state licensure at the time of hire and 4 years of related work experience
    OR


    • Bachelor's Degree or Registered Nurse with current state licensure at the time of hire
    and 1 year of related work experience

    OR


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


    • Licensed Practical Nurse with current state licensure at the time of hire and 5 years of related work experience
    OR


    • Bachelor's Degree or Registered Nurse with current state licensure at the time of hire
    and 2 years of related work experience

    OR


    • Master's Degree in a related field
    and 1 year of related experience


    FOR ALL LEVELS:
    Spanish language fluency-oral and written

    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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