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    Staff Research Associate/Study Coordinator 2 - 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

    Fully On-Site

    Work Schedule

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

    Posted Date

    04/19/2024


    Salary Range:
    $ Hourly

    Employment Type


    • Staff: Career
    Duration

    Indefinite

    Job #

    8438

    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.


    Under the guidance of the Principal Investigator, you'll be responsible for a wide variety of image post-processing and measurement activities.

    You will facilitate the seamless acquisition of laboratory animals and vital experiment supplies while meticulously organizing image measurements within a structured database.

    You will develop summary tables and enter data into a dynamic database to provide the research team with a vital layer of precision for their critical work.

    This role offers the opportunity for exceptional growth and development as you collaborate with world-class research professionals.


    Salary:
    $ $45.11/hour

    Job Qualifications

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

    • Knowledge of health services or clinical research methodology and principles
    • Computer proficiency with Microsoft Word/Excel/Publisher/Access
    • In-depth understanding of Human Subject Protection and informed consent
    • Experience following strict research imaging protocols and data entry
    • Outstanding communication skills
    • Experience working with a diverse research population
    • Knowledge or experience in working with large animals
    • California phlebotomy certification, ACRP or SoCRA highly desirable
    • Bachelor's or Master's degree or related research or analytical experience preferred
    • Knowledge of basic statistical tests and procedures preferred
    • Background in data management of clinical research protocols preferred
    • Prior IRB experience and coordination of clinical studies desired
    • RN licensure a plus
    *
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