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    Clinical Research Coordinator - Oklahoma City, United States - Oklahoma Medical Research Foundation

    Oklahoma Medical Research Foundation
    Oklahoma Medical Research Foundation Oklahoma City, United States

    4 weeks ago

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    Paid Work
    Description

    This job was posted by : For more information,
    please see:

    r

    rClinical Research Coordinator

    r

    rOverview

    rFounded in 1946, the Oklahoma Medical Research Foundation
    (OMRF){target="_blank"
    rel="noopener"} is among the nation\'s oldest, most respected
    independent, nonprofit biomedical research institutes. OMRF is dedicated
    to understanding and developing more effective treatments for human
    diseases, focusing on critical research areas such as Alzheimer\'s
    disease, cancer, lupus, Multiple Sclerosis, and cardiovascular disease.
    OMRF follows an innovative cross-disciplinary approach to medical
    research and ranks among the nation\'s leaders in patents per scientist.

    Located in Oklahoma City, a city that offers a dynamic and flourishing
    downtown area, with low cost of living, short commute times and a
    diversified economy, OMRF has been voted one of the Top Workplaces since
    the inception of the award. This achievement has been accomplished
    thanks to OMRF individuals who share a unified understanding that our
    excellence can only be fully realized with a commitment to diversity,
    equity, and inclusion. Successful candidates will demonstrate commitment
    to these values.

    Benefits

    We offer competitive salaries and comprehensive benefits including,
    medical, dental, and vision insurance, minimum 8% company retirement
    contribution, vacation and sick leave, paid holidays, onsite cafe, free
    onsite fitness center with access to personal trainer, free parking and
    much more Relocation assistance available for those located 50 miles
    outside of Oklahoma City metro and out of state. Learn more about our
    benefits
    here{target="_blank"
    rel="noopener"}.

    OMRF is an Equal Opportunity/Affirmative Action/Veterans Employer. All
    qualified applicants will receive consideration for employment without
    regard to gender, sexual orientation, gender identity, race, color,
    national origin, age, religion, disability, veteran status, or any other
    legally protected characteristic.

    r

    rResponsibilities

    rThe Arthritis and Clinical Immunology Research
    Program{target="_blank"
    rel="noopener"} is seeking enthusiastic, hard-working, fast-learner who
    wants to make a difference, providing novel care options to patients
    with CNS autoimmune diseases, like multiple sclerosis and neuromyelitis
    optica.

    Duties include:

    • Coordinating and maintaining all documentation in accordance with
      and assuring compliance with research and clinical trial regulations
      and protocols. Preparing, submitting, and monitoring documentation
      and changes for Institutional Review Board (IRB) and HIPAA issues,
      rules and regulations including applications for new grants, yearly
      progress renewal reports, and correspondence.
    • Overseeing and/or assisting with clinical trials including
      identifying and recruiting appropriate study patients and controls,
      performing training in a timely fashion, performing phlebotomy,
      initial blood processing/shipping, completing study-specific forms,
      using study-specific databases, reporting adverse events, and
      negotiating budgets. Assuring compliance with regulations and
      protocols through process audits. Overseeing maintenance of cash
      flow records and payments to patients and study participants.
    • Assisting with NIH and other grant applications and renewals by
      overseeing verification of appropriate use of human subjects,
      pulling summary data and assisting with supplementary information
      such as compiling summary data of patient demographics, c mmon
      medications, disease activity measurements, co-morbidities and
      patient reported outcomes.
    • Overseeing and conducting medical record reviews and performing data
      abstraction for disease diagnosis with clinical oversight.
      Overseeing maintenance of internal quality control on chart data
      abstractions.
    • Assisting patients with completion of forms, reviewing forms for
      completeness, making copies, and providing reminder calls about
      clinical research visits.
    • Assisting clinic physicians and other staff as needed. Preparing
      participants for examinations, tests or treatments and explains
      procedures. Performing phlebotomy and basic sample processing as
      needed.
    • May supervise clinical employees and delegate assignments as
      appropriate.
    • Performing other duties as assigned by supervisor.

    r

    rQualifications

    rrrrBachelors degree in healthcare, biosciences or clinical research
    related field with at least 1 year of experience.Knowledge of clinical
    environment including ability to identify basic medical terminology and
    extract information from medical charts. Perform medical procedures like
    vital signs and phlebotomy. Knowledge of applicable computer software
    and databases. Knowledge of HIPAA and IRB rules and regulations.
    Excellent communication skills (both oral and written). Ability to lead,
    supervise and delegate. Ability to identify emergency medical situations
    and follows pro


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