• Sr. Medical Analyst, RWD

    Norstella (Topeka, KS)
    …unites best-in-class brands to help clients navigate the complexities at each step of the drug development life cycle -and get the right treatments to the right ... via our market-leading brands, we help our clients: + Citeline - accelerate the drug development cycle + Evaluate - bring the right drugs to market + MMIT -… more
    Norstella (10/28/25)
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  • Sr. Scientist, Radiopharmaceutical…

    Bristol Myers Squibb (San Diego, CA)
    development , translating cutting-edge scientific discoveries into robust clinical drug products. The Sr. Scientist will lead CMC radiopharmaceutical process ... Process Development & Scale-Up: Drive CMC process development and optimization for clinical drug products,...CMC process development and optimization for clinical drug products, including formulation lock and robust process definition,… more
    Bristol Myers Squibb (12/15/25)
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  • Sr. Scientist, Statistical Programmer, Late Stage…

    Merck (North Wales, PA)
    …This position supports statistical programming activities for late stage drug /vaccine clinical development projects. This may include leadership ... and process compliance. Strong working knowledge of reporting processes (SOPs) and software development life-cycle (SDLC) + US and/or worldwide drug or vaccine… more
    Merck (12/02/25)
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  • Senior Director, Product Management Team Lead…

    Gilead Sciences, Inc. (Foster City, CA)
    Development teams + Deep understanding of all aspects of early drug development + Early-stage development : IND-enabling studies, translational science, ... and manufacturing timelines. + Possess strong business acumen to align drug development and launch strategies with commercial goals, assess financial… more
    Gilead Sciences, Inc. (11/06/25)
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  • Associate Director, Clinical Sciences, Internal…

    Regeneron Pharmaceuticals (Tarrytown, NY)
    …life science/healthcare preferred (PhD/PharmD/MSc). ≥ 10 years of pharmaceutical clinical drug development experience, including basic knowledge of Metabolic ... disease areas. We are seeking proficient knowledge of the drug development process, Good Clinical Practice, study design, clinical research methodology… more
    Regeneron Pharmaceuticals (10/21/25)
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  • Assembler/Tester Sr. - 2nd Shift - Military Flight…

    Parker Hannifin Corporation (Irvine, CA)
    …member competencies and participate in goal setting, performance feedback, and self- development activities. DRUG -FREE WORKPLACE In accordance with Parker's ... a career at Parker presents unlimited opportunities for both professional and personal development . Working with some of the most brilliant minds in the industry,… more
    Parker Hannifin Corporation (12/13/25)
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  • Sr. Manager, Regulatory Affairs Strategy

    Taiho Oncology (Princeton, NJ)
    …directs global regulatory affairs activities and provides regulatory guidance during drug development , approval and post approval processes and ... accessing documentation utilizing multiple electronic systems. + Knowledge of the drug development process, drug laws, global regulations and requirements +… more
    Taiho Oncology (12/13/25)
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  • GMP Manufacturing Technician

    Astrix Technology (Los Angeles, CA)
    …**Why Join?** + Opportunity to work with a dynamic team supporting innovative clinical drug development . + Hands-on experience in a pilot-scale drug ... This role will be based onsite at their pilot-scale drug product manufacturing facility and formulation development ...pilot-scale drug product manufacturing facility and formulation development lab in Thousand Oaks, CA. The technician will… more
    Astrix Technology (10/12/25)
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  • Principal Research Scientist - Modeling…

    AbbVie (Irvine, CA)
    …comfortable with exploratory analyses and non-conventional modeling beyond systemic drug development including ophthalmology, and aesthetics/dermatology. This ... correspondences. + Exploratory analyses and non-conventional modeling beyond systemic drug development with a focus on locally-administered/acting products.… more
    AbbVie (12/10/25)
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  • Senior Manager, Global Product Quality - Biologics

    Otsuka America Pharmaceutical Inc. (Baton Rouge, LA)
    …and performing root cause analysis. + Thorough understanding of GMP requirements and the Drug Development process. + Knowledge of FDA 21 CFR Parts 210 and ... for Otsuka's patients. **Job Description** + Provides Biologics QA support for Drug Substance and Drug Product, including upstream and downstream biologics… more
    Otsuka America Pharmaceutical Inc. (12/03/25)
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