• Senior Director Global Regulatory Affairs - Global…

    Takeda Pharmaceuticals (Boston, MA)
    …**Requirements/Qualifications:** + Advanced degree in a scientific subject area (eg MSc, PhD , PharmD, MD). BA acceptable with significant Industry experience. + Sr ... Director 12+ years of pharmaceutical industry experience inclusive of 10 years of regulatory experience or a combination of 8+ years of regulatory and related… more
    Takeda Pharmaceuticals (07/18/25)
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  • TA Head of Biostatistics, Neuroscience…

    Sanofi Group (Cambridge, MA)
    …identify, prioritize, and lead key EGDS departmental development initiatives **About You** + PhD in Statistics or Biostatistics with typically at least 12 years of ... pharmaceutical experience in clinical development within pharma or biotech industry, including significant senior-level experience and a strong focus on TA and… more
    Sanofi Group (07/18/25)
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  • Senior Scientist Regulatory Compliance

    Cambrex High Point (High Point, NC)
    …3 years of relevant background/leadership in GXP/QA/regulatory compliant pharmaceutical laboratory environment or Quality Assurance/Regulatory Affairs role (prefer ... late phase/commercial experience). Knowledge of GMP manufacturing and analytical techniques to support QA and Regulatory process. Expertise in creating and interpreting SOPs. Ability to function as technical expert/consultant. Sedentary work, exerting up to 10… more
    Cambrex High Point (07/17/25)
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  • Senior Consultant, Evidence Synthesis, Indirect…

    IQVIA (Durham, NC)
    …EXPERIENCE, TECHNICAL AND PERSONAL SKILLS** + **Masters (required) or PhD (preferred) in epidemiology, pharmacology, public health, or biostatistics (other ... of working in evidence synthesis research, preferably in consulting, pharmaceutical or other healthcare industry, academia** + **Substantial experience independently… more
    IQVIA (07/17/25)
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  • Director - Experienced Discovery Toxicology…

    Lilly (Indianapolis, IN)
    …leading toxicology projects to support the discovery and development of new pharmaceutical products while working closely with cross-functional teams to ensure the ... or challenges that arise during the course of toxicology studies. **Minimum Requirements:** PhD in Toxicology, Pathology or related field with 7+ years of relevant… more
    Lilly (07/16/25)
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  • Research Associate

    University of Maryland, Baltimore (Baltimore, MD)
    …procedures. * Perform other duties as assigned. *_QUALIFICATIONS_* * PhD in Neuroimaging (including focused ultrasound), Neuroscience, Engineering, Molecular ... Biology, Pharmaceutical Sciences, Toxicology, or a related field. * A minimum of three years post-doctoral training (or equivalent) is desired. * The candidate must… more
    University of Maryland, Baltimore (07/16/25)
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  • Research Associate

    University of Maryland, Baltimore (Baltimore, MD)
    …other projects in the laboratory on an occasional basis. *Qualifications* PhD in Materials Science and Engineering, Chemistry, Bioengineering, Chemical Engineering, ... Pharmaceutical Sciences, or a closely related field. Candidates must have strong work ethic, and possess technical, critical thinking, interpersonal and written… more
    University of Maryland, Baltimore (07/16/25)
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  • Manager, Regulatory Affairs Advertising…

    Gilead Sciences, Inc. (Foster City, CA)
    …and enforcement actions with regards to advertising and promotion of pharmaceutical products. + May initiate and/or contribute to local process improvements ... and skills we seek for this role. **Education & Experience** + PharmD/ PhD with some relevant experience. + MA/MS/MBA with 4+years' relevant experience. +… more
    Gilead Sciences, Inc. (07/16/25)
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  • US Tech Consultant / Senior Consultant - Insights…

    Blue Matter (San Francisco, CA)
    …and Skills + Expertise in data engineering/analytics/Gen AI application development for pharmaceutical datasets. + Expertise in SQL, Python and databases (eg, MySQL, ... presentation skills (internal and client facing) Preferred Qualifications: + Advanced degree(s) ( PhD , MD, MBA, or MS) + 4 years of quantitative analytical experience… more
    Blue Matter (07/16/25)
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  • Future Opportunities- Join Our Talent Pipeline…

    AbbVie (Mettawa, IL)
    …English or communications, with significant relevant science experience. Masters or PhD in science discipline preferred with relevant writing experience. + American ... (AMWA) certification or other is preferred, with a specialty in Editing/Writing or Pharmaceutical . + 4 years relevant industry experience in medical writing in the… more
    AbbVie (07/14/25)
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