• Sr Director , Project Management,…

    ThermoFisher Scientific (Greenville, NC)
    …deliverables + Advanced, broad understanding of global/regional/national country requirements/ regulatory affairs procedures for clinical trial authorization, ... of ICH and other global regulatory guidelines; in-depth understanding of a regulatory specialty areas, such as preclinical, clinical, CMC , publishing, etc. +… more
    ThermoFisher Scientific (12/03/25)
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  • Sr Oversight Director , Project Management…

    ThermoFisher Scientific (Greenville, NC)
    …deliverables + Advanced, broad understanding of global/regional/national country requirements/ regulatory affairs procedures for clinical trial authorization, ... of ICH and other global regulatory guidelines; in-depth understanding of a regulatory specialty areas, such as preclinical, clinical, CMC , publishing, etc. +… more
    ThermoFisher Scientific (10/15/25)
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  • Instructor for Master of Science (MS)…

    University of Maryland, Baltimore (Baltimore, MD)
    …in the MS in Regulatory Science program, with a focus on introductory and regulatory affairs aspects of the program, as well as another aspect of the program ... AREAS OF EXPERTISE AND EXPERIENCE_* Regulatory science, including introductory and regulatory affairs aspects, as well deep knowledge in another aspect (eg… more
    University of Maryland, Baltimore (10/14/25)
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  • Process Scientist (Associate Director )…

    Takeda Pharmaceuticals (Boston, MA)
    …+ Manufacturing Sciences + Global Manufacturing Supply, Global Quality and Global Regulatory Affairs . + SME for Takeda drug product manufacturing organization ... **Location: Cambridge, MA** **About the role:** As a Process Scientist (Associate Director ) - Global Manufacturing Science GMSci Drug Product (DP), you will provide… more
    Takeda Pharmaceuticals (09/20/25)
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  • Senior Scientific Director , Clinical…

    AbbVie (Irvine, CA)
    …required by program needs, in partnership with Discovery, Translational, and CMC colleagues contribute to design and implement translational strategies. May ... opinion leader interactions related to the disease area(s); partners with Medical Affairs , Commercial and other functions in these activities as required, consistent… more
    AbbVie (11/07/25)
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  • Sr. Manager, Supply Chain

    Mitsubishi Chemical Group (Jersey City, NJ)
    …by closely working with MTP internal colleagues in various functions (Quality Assurance, Regulatory Affairs , Marketing, Market Access, Medical Affairs , Drug ... effectively with colleagues in Supply Chain, Accounting, Market Access, Quality Assurance, Regulatory Affairs , Finance, etc. of Tanabe Pharma Group, including… more
    Mitsubishi Chemical Group (09/24/25)
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  • Clinical Study Physician

    Teva Pharmaceuticals (Parsippany, NJ)
    …and Teva Standard Operating Procedures + Partners cross-functionally with departments such as Regulatory Affairs , CMC , Biostatistics, GCO, in the execution ... Clinical Scientist. and other functional areas such as GCO, biostats, regulatory , pharmacovigilance. The Director will be a key contributor to INDs, NDAs, BLAs,… more
    Teva Pharmaceuticals (10/07/25)
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