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    Clinical Trials Regulatory Coordinator - 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 8am - 5pm (hours may vary)
    Posted Date
    01/29/2024

    Salary Range:
    $ Hourly

    Employment Type

    • Staff: Career
    Duration
    Indefinite
    Job #
    12279
    Primary Duties and Responsibilities
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    The Department of Urology is seeking to hire a full time Clinical Trails Regulatory Coordinator to be responsible for regulatory coordination of clinical research studies within assigned units at the Institute of Urologic Oncology


    Main responsibilities include:

    • Performing detailed review of clinical research protocols and utilizing that information to prepare, manage and submit all required study/regulatory documents and all required applications and forms related to internal UCLA requirements, FDA requirements, sponsor requirements, etc.
    • Working with study monitors to process, review and collect the appropriate regulatory documents in a timely manner and in compliance with federal, state, and university mandated laws, regulations and policies.

    Pay Range:
    $ $59.34 hourly.

    Job Qualifications
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    Preferred:
    Associate's or Bachelor's Degree.

    Required:
    1+ years of Clinical Research experience.
    High School Diploma.

    Interpersonal skills to effectively communicate information in a timely, professional manner and establish and maintain cooperative and effective working relationships with students, staff, faculty, external collaborators and administration and to work as a member of a team.

    Ability to set priorities and complete ongoing tasks with competing deadlines, with frequent interruptions, to meet the programmatic and department needs, while complying with applicable University policies and federal and state regulations.

    Analytical skills to assess clinical research protocols and regulatory requirements, define problems, formulate logical solutions, develop alternative solutions, make recommendations, and initiate corrective actions.

    Close attention to detail to ensure accuracy in a fast-paced, fluctuating workload environment.

    Organization skills to create and maintain administrative and regulatory files effectively as well as independently balance the various tasks to ensure deadlines are met.

    Demonstrated proficiency with Adobe and Microsoft suite software, especially Excel, to perform daily tasks efficiently and accurately.

    A learning and professional growth mentality so that new software tools, systems, and processes can be adopted quickly and efficiently.

    Working knowledge of clinical research concepts, policies and procedures, and human safety protection regulations and laws.

    Knowledge of and experience working with a variety of local and external IRBs, scientific review and other research committees, national cooperative group sponsors, industry sponsors, federal and foundation funding organizations, etc.

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