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    Research Coordinator - Los Angeles, United States - UCLA Health

    UCLA Health
    UCLA Health Los Angeles, United States

    1 week ago

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    Description
    General Information

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    Work Location:
    Los Angeles, USA

    Onsite or Remote

    Flexible Hybrid

    Work Schedule

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

    Posted Date

    02/22/2024


    Salary Range:
    $ Hourly

    Employment Type


    • Staff: Limited
    Duration

    3 months

    Job #

    12674

    Primary Duties and Responsibilities

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    The Department of Medicine is seeking to hire a Clinical Research Coordinator to play a key role in managing all aspects of clinical research activities.

    From inception to completion, this position oversees the operational aspects of trials, ensuring adherence to protocols and regulatory requirements, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP).

    Responsibilities include implementing research plans, managing project tasks, and coordinating with various stakeholders such as Principal Investigators, sponsors, and institutional teams.

    The ideal candidate will prioritize tasks effectively, maintain compliance with regulations, and support the successful administration of research projects.


    • Note this a limited role which may convert to careerHourly range: $32.65-$52.53
    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 respond to situations in an appropriate and professional manner.
    • 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

    Preferred:

    • Strong verbal and written communication skills along with strong interpersonal skills to effectively establish rapport, and build collaborate relationships.
    • Strong organizational capabilities to organize multiple projects and competing deadlines for efficiency and cost-effectiveness.
    • Working knowledge of the clinical research regulatory framework and institutional requirements.
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