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    Clinical Research Coordinator, CARE Center - Los Angeles, United States - UCLA Health

    UCLA Health
    UCLA Health Los Angeles, United States

    2 weeks ago

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    Description
    General Information

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    Work Location:
    Los Angeles, USA

    Work Schedule

    Monday - Friday, 8:00am - 5:00pm

    Posted Date

    12/04/2023


    Salary Range:
    $ Hourly

    Employment Type


    • Staff: Career
    Duration

    Indefinite

    Job #

    3073

    Primary Duties and Responsibilities

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    As the Clinical Research Coordinator for the Department of Medicine, CARE Center, you will be responsible for performing research activities directly related to HIV clinical trials and COVID-19 clinical trials


    Duties include:

    • Coordinate activities for clinical research studies, such as participant recruitment and enrollment; data management; and education as related to each protocol
    • Document signs, symptoms and other changes with research patients
    • Assist with preparing reports and submissions
    • Participate in quality assurance activities for studies across the research unit
    • Work with outreach team in expanding recruitment efforts for COVID-19 and HIV trials

    Salary range:
    $32.65-$52.53 Hourly

    Job Qualifications

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    Required:

    • Analytical skills sufficient to work and solve address problems and identify solutions with reasoned judgment.
    • Ability to adapt to changing job demands and priorities; work flexible hours to accommodate research deadlines.
    • Ability to concentrate and focus in a work environment that contains distracting stimuli and competing deadlines.
    • Ability to be flexible in handling work delegated by more than one individual.
    • Typing and computer skill/ability including word-processing, use of spreadsheets, email, data entry. Ability to navigate numerous software programs and applications.
    • Ability to handle confidential material information with judgement and discretion.
    • Mathematical skills Sufficient to prepare clinical research budgets, knowledge of math ability and knowledge of clinical trials research budgeting process to assist with the preparation of clinical trial budgets.
    • Working knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice (GC) for clinical research.
    • Be available to work in more than one environment, travel to meetings, off-site visits, conferences, etc.
    • Bachelors Degree or 1-3 years of previous study coordination or clinical research coordination experience
    • Strong verbal and written communication skills along with strong interpersonal skills to effectively establish rapport, and build collaborate relationships.
    • Working knowledge of the clinical research regulatory framework and institutional requirements.
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