Expert Veeva EDC Programmer - Eluru - SIRO

    SIRO
    SIRO Eluru

    1 week ago

    Description

    As a key player in Clinical Information Operations, you will create eCRF specifications, design, develop and validate clinical trial setup process.

    • Create edit check specifications and setup edit checks at trial level
    • Implement UAT scripts to test the setup of the clinical study
    • Setup different instances of study URL(eg: UAT, production, testing etc.,)

    You will also be responsible for setting up user accounts for study teams.

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