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    Clinical Researcher Coordinator - Los Angeles, United States - UCLA Health

    UCLA Health
    UCLA Health Los Angeles, United States

    1 day ago

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    Description
    General Information

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    Work Location:
    Los Angeles, USA

    Onsite or Remote

    Fully Remote

    Work Schedule

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

    Posted Date

    12/04/2023


    Salary Range:
    $ Hourly

    Employment Type


    • Staff: Career
    Duration

    Indefinite

    Job #

    11009

    Primary Duties and Responsibilities

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    Ready to take charge in the world of clinical research? As a Clinical Research Coordinator, you'll be at the forefront of managing the entire journey of research projects, from conception to completion.

    Your role involves implementing multiple studies, juggling tasks to meet crucial deadlines, and ensuring strict adherence to study protocols and regulations.

    Collaboration is key as you work alongside the Principal Investigator, various departments, sponsors, and more, ensuring studies run smoothly, stay compliant, and receive the support they need.

    Join us in shaping the future of clinical research with precision and impact.


    Salary:
    $ $52.53/hour

    Job Qualifications

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    Required:

    • Strong verbal and written communication skills along with strong interpersonal skills to effectively establish rapport, and build collaborative relationships.
    • Strong organizational capabilities to organize multiple projects and competing deadlines for efficiency and cost-effectiveness.
    • 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.
    • Typing and computer skill/ability including word-processing, use of spreadsheets, email, data entry.

    Preferred:

    • Bachelors Degree or 1-3 years of previous study coordination or clinical research coordination experience
    • Working knowledge of the clinical research regulatory framework and institutional requirements.
    • 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.
    • Fluent in writing and speaking Spanish.
    • Demonstrated skills in using PC computer, MS Word, MS Excel, PowerPoint, Internet and Windows applications.
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