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    Clinical Study Initiation Analyst - Los Angeles, United States - UCLA Health

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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, 7:00am - 4:00pm

    Posted Date

    04/29/2024


    Salary Range:
    $ Hourly

    Employment Type


    • Staff: Career
    Duration

    Indefinite

    Job #

    15294

    Primary Duties and Responsibilities

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    Under the direction of the Clinical Study Initiation Manager (CSI Manager) and the Sr.

    Research Manager, the JCCC Director, the JCCC Chief Administrative Officer (CAO), the JCCC Senior Director of Clinical Oncology Research and TRIO-US Network and the CRU Medical Director (Senior Leadership), the Clinical Study Initiation (CSI) Analyst is required to do database management, with regards to research trials and patient information, build/update research calendar specification calendars and budgets, as well as ensure the integrity of data being collected and entered into the clinical research management system (CRMS).

    The position will be responsible for creating and updating study protocol calendars and budgets. In addition, the incumbent will monitor, verify and validate the integrity of various data elements into the CRMS.


    Salary:
    $ $59.34 hourly

    Job Qualifications

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    Required:

    • Excellent written and verbal communication skills
    • Proficiency in Windows, MS Office applications in particular Excel and Word.
    • Strong demonstrated problem-solving skills, critical thinking and the ability to complete job responsibilities with minimal supervision.
    • Strong interpersonal skills and ability to interact professionally and appropriately with both faculty, staff and external partners.
    • Skill in multi-tasking, prioritizing job responsibilities while maintaining accuracy and efficiency.
    • Highly organized and detailed with impeccable follow-through.

    Preferred:

    • Experience working in the clinical research field.
    • Experience using OnCore or other Research Management Systems (CRMS).


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