• Associate Principal Scientist

    Merck (Austin, TX)
    … updates. + Audit vendors/partners of SaMD/IVD/Companion Diagnostics **Reports to** - Director Regulatory Compliance, Device Quality and Regulatory ... This position will be part of the Device Quality & Regulatory Team within Global Regulatory Affairs and Clinical Safety (GRACS). The primary responsibility for… more
    Merck (06/24/25)
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  • Senior Principal Research Scientist

    AbbVie (North Chicago, IL)
    …LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description Purpose: The Senior Principal Research Scientist / Director of Drug Metabolism and ... of absorption, distribution, metabolism, excretion (ADME), and pharmacokinetics. + Ensure regulatory compliance for all studies and reports, providing oversight of… more
    AbbVie (06/06/25)
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  • Senior Principal Scientist

    Bristol Myers Squibb (Cambridge, MA)
    …track record of high-quality scientific publications in relevant fields For the Sr. Principal Scientist position, the starting compensation for this job is a ... oncology. + Manage relationships with key internal stakeholders including regulatory , clinical and commercial and scientific communications and external… more
    Bristol Myers Squibb (06/23/25)
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  • Associate Director / Principal

    Gilead Sciences, Inc. (Foster City, CA)
    …Join Gilead and help create possible, together. **Job Description** The Associate Director / Principal Scientist , Cell Culture Process Development (Pivotal & ... development, platform process evolution, and to support cell culture-related regulatory documentation. **Key Responsibilities:** + Optimize and characterize cell… more
    Gilead Sciences, Inc. (06/11/25)
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  • Principal Scientist , Analytical…

    Catalent Pharma Solutions (Baltimore, MD)
    …on Quality by Design principles and regulatory compliance. The Principal Scientist will report to the Senior Director of Analytical Development and is ... ** Principal Scientist , Analytical Development** **Summary:** Catalent...Scientist - Analytical Development will report to the Senior Director , Analytical Development. **Catalent is committed to a Patient… more
    Catalent Pharma Solutions (06/13/25)
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  • Principal Scientist , Analytical R&D

    Merck (Rahway, NJ)
    **Job Description** ** Principal Scientist , Small Molecule Analytical Research & Development** The Small Molecule Analytical Research and Development (SMAR&D) ... group has an exciting opportunity for a Principal Scientist based in Rahway, NJ. Join...sterile and combination products. You will also contribute towards regulatory submissions to enable clinical trials. Your main responsibilities… more
    Merck (06/03/25)
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  • Principal Scientist , Clinical…

    Merck (Rahway, NJ)
    **Job Description** The Director ( Principal Scientist ) has primary responsibility for the planning and directing clinical research activities involving new ... cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, The Director May… more
    Merck (06/24/25)
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  • Principal Scientist , Analytical R&D…

    Merck (Rahway, NJ)
    …of our company's Research Laboratories Division is seeking applicants for a Principal Scientist position available at our company's research facility. The ... Principal Scientist is a senior scientific role tasked with working closely with the group Director to define group strategy and to lead a team of scientists… more
    Merck (04/26/25)
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  • Senior Principal Scientist

    Merck (Rahway, NJ)
    …and pipeline products to produce safe, effective, innovative medicine. The Senior Principal Scientist /Senior Director is responsible for protocol development ... of manuscripts for publication in peer-reviewed journals. The Senior Director will also contribute to establishing Vaccine Clinical Development Strategies… more
    Merck (06/10/25)
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  • Regulatory Scientist I / II…

    UTMB Health (Galveston, TX)
    Regulatory Scientist I / II - Institutional Office... Scientist II will be assigned as a Study Director , as defined by the US FDA Good Laboratory Practice ... for the interpretation, documentation and reporting of results. The Regulatory Scientist I / II works in...I / II works in conjunction with the Scientific Director for the Institutional Office of Regulated Nonclinical Studies… more
    UTMB Health (04/23/25)
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