• Adverse Event Reporting…

    Terumo Medical Corporation (Elkton, MD)
    Adverse Event Reporting Spec II Date: Jan 7, 2026 Req ID: 5444 Location: Elkton, MD, US Company: Terumo Medical Corporation Department: Post Market ... US and global health authorities (GHA) such as FDA, HC, MHRA, etc. The Adverse Event Reporting Team is responsible with implementation of best practices to… more
    Terumo Medical Corporation (01/08/26)
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  • Human Subject Research Spec I

    University of Rochester (Rochester, NY)
    …procedures, study activities, source documentation and case report form (CRFs) completion, and adverse event reporting . + Reviews and documents the ... use of device, and/or other interventional activities, to document adverse events and report to senior study staff, PI,...questions that arise during the study, communicates and documents adverse events as advised by the PI and ensures… more
    University of Rochester (11/27/25)
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  • Senior Researcher - Ops, Consumer Insights,…

    Amazon (Culver City, CA)
    …and international markets, adapting to regional requirements and cultural considerations -Create spec memos and questionnaires for each screening event , ensuring ... in research operations, film production operations, or entertainment industry event management * Proven track record managing large-scale, high-profile screening… more
    Amazon (12/23/25)
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