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    Clinical Research Coordinator - Norman, United States - The University of Oklahoma

    The University of Oklahoma
    The University of Oklahoma Norman, United States

    1 day ago

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    Description

    Identifies and assesses patients who may be eligible to participate in a clinical trial or research program, distributes information, acts as a clinical resource, manages data, conducts follow-up care for patients, and attends meetings pertaining to the program.


    Duties:

    • Identifies patients who may be eligible to participate in a clinical trial or research program.
    • Performs the initial assessment of potential patients.
    • Takes clinical history and completes patient data forms.
    • May perform a physical exam during the assessment.
    • Provides potential patients with study information.
    • Obtains informed consent forms.
    • Acts as a clinical resource and liaison between physicians, nurses, and laboratory personnel.
    • Assists in data management and data analysis.
    • Responsible for the initiation, organization, and carrying out of patient follow-up.
    • Assesses patient at all follow-up visits.
    • Attends various meetings pertaining to the clinical trial or research program.
    • May present information.
    • May train clinical research staff.
    • Performs various duties as needed to successfully fulfill the function of the position.

    Education:
    Bachelor's Degree


    • 12 months of clinical practice, nursing, or clinical trial or research program coordination experience

    Equivalency/Substitution:
    Will accept 48 months of equivalent experience in lieu of a Bachelor's Degree for a total of 60 months experience or a Master's Degree in lieu of experience


    Certifications/Licenses:

    • Oklahoma State licensure is required for Nurses and Physician Assistants
    • Basic Life Support (BLS) or able to obtain within 30-days from hire date

    Skills:

    • Knowledge of clinical trial protocols
    • Ability to communicate verbally and in writing
    • Ability to explain the clinical trial study information to the participants
    • Ability to read and follow instructions and guidelines

    Preferred:

    • 24 months of clinical practice, nursing, or clinical trial or research program coordination experience

    Working Conditions:

    • Physical: Sitting for prolonged periods, manual dexterity, speaking and listening, reaching, bending, standing and stooping.
    • Environmental: Clinic environment, exposure to infectious diseases.

    Equal Employment Opportunity Statement:

    The University of Oklahoma, in compliance with all applicable federal and state laws and regulations, does not discriminate on the basis of race, color, national origin, sex, sexual orientation, genetic information, gender identity, gender expression, age, religion, disability, political beliefs, or status as a veteran in any of its policies, practices, or procedures.

    This includes, but is not limited to, admissions, employment, financial aid, housing, services in educational programs or activities, and health care services that the University operates or provides.


    Diversity Statement:

    The University of Oklahoma is committed to achieving a diverse, equitable, and inclusive university community by recognizing each person's unique contributions, background, and perspectives.

    The University of Oklahoma strives to cultivate a sense of belonging and emotional support for all, recognizing that fostering an inclusive environment for all is vital in the pursuit of academic and inclusive excellence in all aspects of our institutional mission.

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