• Merck & Co. (North Wales, PA)
    …portfolio and compliance with public disclosure of clinical trials and their results. The Senior Informed Consent Medical Writer is responsible for ... internal policy, regulatory requirements, and health literacy principles.With minimal oversight, the Senior Informed Consent Medical Writer:Demonstrates… more
    HireLifeScience (06/06/25)
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  • Merck & Co. (North Wales, PA)
    …portfolio and compliance with public disclosure of clinical trials and their results. The Senior Informed Consent Medical Writer is responsible for ... policy, regulatory requirements, and health literacy principles.With oversight, the Informed Consent Medical Writer:Demonstrates growing independence… more
    HireLifeScience (06/06/25)
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  • Sr . Informed Consent

    Merck (North Wales, PA)
    …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 (North Wales, PA)
    …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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  • Late Stage Oncology Clinical Scientist

    Pfizer (Collegeville, PA)
    …other clinical and medical colleagues, with authoring protocols, study level informed consent documents, site training materials, and other clinical and ... disease area(s) of assignment. + Support other clinical and medical colleagues, clinical operations and other functional lines for...of the drug, keeping the clinical and safety colleagues informed of changes in the safety profile as they… more
    Pfizer (06/07/25)
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  • Late Stage Oncology Clinical Scientist

    Pfizer (Collegeville, PA)
    …integrity and quality of the clinical trial(s). + Authors protocols, study level informed consent documents, and contributes to authoring of IBs, site training ... area(s) of assignment. + Partners with other clinical and medical colleagues, clinical operations and other functional lines for...of the drug, keeping the clinical and safety colleagues informed of changes in the safety profile as they… more
    Pfizer (05/29/25)
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