• Process Development Senior Scientist

    Amgen (Thousand Oaks, CA)
    …Amgen's Commercial Attribute Sciences group in Thousand Oaks, California is seeking a Principal Scientist . The successful candidate will join us on our effort ... lasting impact on the lives of patients as we research , manufacture, and deliver innovative medicines to help people...of patients while transforming your career. **Process Development Senior Scientist ** **What you will do** Let's do this. Let's… more
    Amgen (11/20/25)
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  • Highly Distinguished/ Distinguished…

    Boehringer Ingelheim (Ridgefield, CT)
    …act as internal expert in toxicology across therapeutic areas. The Highly Distinguished Research Scientist needs to have deep understanding about what is ... ( principal author) and at least 10 years of experience in pharmaceutical R&D with track record of independent research **Highly Distinguished Fellow:**… more
    Boehringer Ingelheim (11/28/25)
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  • Senior Director, Clinical Research

    Merck (Rahway, NJ)
    **Job Description** The Senior Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing clinical research activities ... Clinical Trials Monitoring, General Cardiology, Medical Monitoring, Medical Training, Pharmaceutical Industry, Pharmaceutical Medicine, Research Activities… more
    Merck (11/22/25)
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  • Bioassay - Technical/Scientific

    Charles River Laboratories (Ashland, OH)
    …+ Independently ensure scientific integrity of studies.Independently function as a Principal Investigator, Individual Scientist , or Project Scientist ... can feel passionate about. **Job Summary** Serve as a scientist in the conduct of assigned nonclinical or clinical...9 to 12 years related experience in the contract research , academic, or pharmaceutical industry. + Practical… more
    Charles River Laboratories (10/14/25)
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  • Director, Early Clinical Development (MD)…

    Bristol Myers Squibb (Princeton, NJ)
    … industry preferred OR + Significant independent clinical/laboratory/translational research experience in academic/ pharmaceutical setting preferred including ... on Clinical Trial data to support development, and + Serving as principal functional author for Regulatory submission, study reports, and publications + Provides… more
    Bristol Myers Squibb (11/21/25)
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  • Associate Director. Technical Project Management

    Merck (Boise, ID)
    …Under the guidance of dCMC Regulatory Authoring Leadership, the Associate Principal Scientist , Regulatory Authoring Business Owner, will optimize regulatory ... or related field with a minimum of 8 years of experience in the pharmaceutical industry + MS in chemistry, engineering, or related field with a minimum of… more
    Merck (11/27/25)
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