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    Staff Research Associate/ Study Coordinator 3 - Los Angeles, United States - UCLA Health

    UCLA Health
    UCLA Health Los Angeles, United States

    3 weeks ago

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    Description
    General Information

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    Work Location:
    Los Angeles, USA

    Onsite or Remote

    Fully On-Site

    Work Schedule

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

    Posted Date

    04/19/2024


    Salary Range:
    $ Monthly

    Employment Type


    • Staff: Career
    Duration

    indefinite

    Job #

    12255

    Primary Duties and Responsibilities

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    Play a key role with a world-renowned leader in medical research. Help advance medical knowledge and leading-edge patient care. Take your career to a higher level. You can do all this and more at UCLA Health.

    As a Study Coordinator in clinical research, you will be responsible for human subject recruitment, screening, enrollment, and retention. The role will involve applying your skills in organizing, analyzing data, generating summary figures, and preparing presentations and manuscripts.

    You will need to be proficient in the use of image post-processing (e.g., MRI, cardiac ultrasound, echo, etc.) and measurements.

    You will also assist with image measurements, database management, and ordering laboratory animals and supplies.


    Salary:
    $64,498 - $103,732 annually

    Job Qualifications

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    We're seeking a self-motivated, independent professional with:

    • Five or more years of experience as a study coordinator for clinical research
    • Data management experience with clinical research protocols
    • Knowledge of health services or clinical research methodology and principles
    • IRB experience and coordination of clinical studies preferred
    • Background in ARC and pre-clinical large animal studies desired
    • Experience following strict research imaging protocols and data entry
    • Exceptional writing skills, including the co-authorship or authorship of research or technical reports
    • Computer proficiency with Microsoft Office, STATA, SAS, Illustrator, Mimics, etc.
    • Familiarity with basic statistical tests and procedures
    • Knowledge of the rules and regulations for Human Subject Protection and informed consent
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