• Technical Writer / Lead

    ThermoFisher Scientific (Mount Prospect, IL)
    …analysis tools (eg, 6M, Fishbone, TapRooT) and general problem-solving techniques. + Lead , initiate, and assist with the completion of immediate corrections and CAPA ... industry. + Minimum of 3 years of experience in technical or scientific writing principles. + Demonstrable knowledge of...to mentor and train others. + Experience with training technical writing skills and Root Cause Analysis Tools preferred.… more
    ThermoFisher Scientific (11/10/24)
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  • Nonclinical Submissions Writer

    J&J Family of Companies (Spring House, PA)
    Johnson & Johnson is recruiting for Nonclinical Submissions Writer , Preclinical Sciences and Translational Safety to join our team located at our Spring House, PA ... potential. At Johnson & Johnson, we all belong. The Nonclinical Submissions Writer will prepare and review regulatory submission documents that summarize toxicology,… more
    J&J Family of Companies (11/13/24)
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  • Grant Writer

    Suny Polytechnic Institute (Utica, NY)
    …and editing of figures and other graphical elements. Work may include being the lead writer on non- technical applications. + Identify resources both internal ... Professional Posted On: Tue Jul 23 2024 Job Description: The Grant Writer will identify funding opportunities, draft proposals, prepare supporting documentation and… more
    Suny Polytechnic Institute (10/24/24)
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  • Executive Director, Global Clinical Lead

    Pfizer (Pearl River, NY)
    **Role Summary** The Global Clinical Lead functions independently and has direct experience with all the steps in designing and delivering results of clinical ... by applying extensive expertise and in-depth knowledge of clinical research to lead global clinical research programs and registration activities across one or more… more
    Pfizer (10/10/24)
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  • Director, Medical Monitor (MD), VRD

    Pfizer (Pearl River, NY)
    …data, and performs review of cumulative safety data with the safety risk lead . + As appropriate, the clinician medical monitor may delegate these responsibilities to ... requirements, clinical plan expectations, and study timelines; this includes ensuring medical/ technical requirements for data integrity are applied. + Works with… more
    Pfizer (11/10/24)
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  • Director

    University of Washington (Seattle, WA)
    …manage the process for submitting a new grant proposal with the assigned PI and grant writer . + 15% Lead and manage all aspects of the UW's internal processes ... functions pertaining to grant administration/compliance and work with the grant Principal Investigator (PI), the UW Office of Sponsored Programs, Grant and Contract… more
    University of Washington (11/01/24)
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  • QC Microbiologist

    Actalent (Parsippany, NJ)
    …LIMS). + Work weekends, overtime, on-call, and holidays as needed. + Serve as Lead investigator and writer for lab-related issues, conduct formal ... for the QC laboratory. This includes conducting laboratory investigations, authoring technical protocols and reports, performing data reviews and trend analyses,… more
    Actalent (11/07/24)
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  • Associate Director, Nonclinical Regulatory Writing…

    Takeda Pharmaceuticals (Lansing, MI)
    …Regulatory Writing and Submission Support, _Oncology and Marketed Products_ . Team lead , based in Cambridge, MA/Virtual. Here, you will be a vital contributor ... Investigational New Drug Applications (INDs), Clinical Trial Applications (CTAs), Investigator 's Brochures (IBs), New Drug Applications (NDAs), Biologic License… more
    Takeda Pharmaceuticals (09/19/24)
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