• Sr . Informed Consent

    Merck (Olympia, WA)
    …portfolio and compliance with public disclosure of clinical trials and their results. The Senior Informed Consent Medical Writer is responsible for ... regulatory requirements, and health literacy principles. **With minimal oversight, the Senior Informed Consent Medical Writer:** + Demonstrates… more
    Merck (06/06/25)
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  • Informed Consent Medical

    Merck (Olympia, WA)
    …portfolio and compliance with public disclosure of clinical trials and their results. The Senior Informed Consent Medical Writer is responsible for ... regulatory requirements, and health literacy principles. With oversight, the Informed Consent Medical Writer: + Demonstrates growing independence managing… more
    Merck (06/06/25)
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  • Senior Clinical Research Monitor

    Edwards Lifesciences (Seattle, WA)
    …to develop process improvements. + Contribute to the development of clinical protocols, informed consent forms, and case report forms, and participate in team ... the trial/study. + Ensure source documentation is properly recorded and edit/amend informed consent documents as needed. + Perform other incidental duties… more
    Edwards Lifesciences (04/23/25)
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  • Associate Medical Director,…

    Sumitomo Pharma (Olympia, WA)
    … safety subject matter expert (SME) on behalf of PVRM for: Study Protocols, Informed Consent Forms (ICF), Safety Management Plans (SMP), Clinical Study Reports ... signal evaluation reports according to established safety governance policies and keeping senior leadership informed of safety issues. **Job Duties and… more
    Sumitomo Pharma (05/16/25)
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