• Merck & Co. (Upper Gwynedd, PA)
    …of the probability of regulatory success together with risk mitigation measures.- Lead development and execution of global product and project regulatory ... strategy(ies) by ensuring robust assessment of global regulatory CMC requirements and critical evaluation of supporting documentation to confirm acceptability… more
    HireLifeScience (07/19/25)
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  • Merck & Co. (South San Francisco, CA)
    …(including discovery research, biostatistics, drug metabolism, modeling and simulation, regulatory affairs, and global clinical trials operations)Provide ... Job Description Senior Principal Scientist Translational Medicine, Immunology Translational Medicine in our Research & Development Division is responsible for… more
    HireLifeScience (07/30/25)
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  • Merck & Co. (Rahway, NJ)
    …ensure full integration of the device development activities with the clinical, regulatory , formulation, commercial and other key company functions. Lead the ... in the design, manufacturing, verification, validation and associated quality and regulatory aspects of combination products.The incumbent must be able to … more
    HireLifeScience (07/29/25)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionDevice Development Associate Principal Scientist - Development Strategy, Design Controls(Associate Director Equivalent) Our company's Device ... from early design concept definition through commercialization to support regulatory filing, product launch, and post-market surveillance.This position will interact… more
    HireLifeScience (07/30/25)
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  • Merck & Co. (North Wales, PA)
    …of clinical/scientific execution of clinical protocol(s). This may include:Serving as the lead clinical scientist on the clinical trial team.Leading medical ... your leadership, technical skills, and scientific acumen as part of a global , cross functional team.Job ResponsibilitiesResponsible for leading specific aspects… more
    HireLifeScience (07/26/25)
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  • Merck & Co. (Rahway, NJ)
    …clinical/scientific execution of clinical protocol(s) . This may include: Serving as the lead clinical scientist on the clinical trial team. Leading medical ... technical skills, and scientific acumen as part of a global , cross-functional team . - Job Responsibilities - Responsible...clinical scientists. Core Skills Solid knowledge of clinical research regulatory requirements (e . g . , GCP and… more
    HireLifeScience (07/24/25)
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  • Associate Principal Scientist

    Organon & Co. (Plymouth Meeting, PA)
    …through the product lifecycle. + Lead development and execution of global product and project regulatory strategy(ies) by ensuring robust assessment of ... regulations and guidances, and Organon procedures. The Associate Principal Scientist will lead the preparation and submission...CMC changes, identification of global regulatory requirements and critical evaluation of… more
    Organon & Co. (07/22/25)
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  • Associate Principal Scientist (Associate…

    Merck (Upper Gwynedd, PA)
    …the probability of regulatory success together with risk mitigation measures. + Lead development and execution of global product and project regulatory ... strategy(ies) by ensuring robust assessment of global regulatory CMC requirements and critical evaluation of supporting documentation to confirm acceptability… more
    Merck (07/19/25)
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  • VP - Regulatory Reporting Ld Analyst / Data…

    Citigroup (Tampa, FL)
    The Global Regulatory and Capital Reporting -...Innovation organization is looking for an Analyst / Data Scientist who is a dynamic individual to help shape ... processes, which then culminates with instituting common and optimized financial / regulatory reporting processes. Global Regulatory and Capital Reporting… more
    Citigroup (06/07/25)
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  • VP Lead Data Scientist

    Wells Fargo (Charlotte, NC)
    We are seeking a visionary and hands-on **Vice President-level Lead Data Scientist ** to join our ** Global Payments & Liquidity (GPL)** team. In this role, ... understand strategic goals and translate them into data science initiatives. + Lead the design and implementation of complex solutions and deliverables by… more
    Wells Fargo (07/19/25)
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  • Senior Scientist Regulatory

    Cambrex High Point (High Point, NC)
    …Start a career where You Matter by applying today! Job Overview The Senior Scientist , Regulatory Compliance will provide oversight of regulatory compliance ... Company Information You Matter to Cambrex. Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance, drug… more
    Cambrex High Point (07/17/25)
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  • Executive Director, Clinical Scientist

    Bristol Myers Squibb (San Diego, CA)
    …and in their personal lives. Read more: careers.bms.com/working-with-us . The **Clinical Scientist Program Lead ** reports through the Clinical Science function ... of innovative protocols and data packages for CSRs and Regulatory Filings. The Program Lead oversees all...a member of the Clinical Science Leadership Team and Global Program Team * Drives resource forecasting, talent development,… more
    Bristol Myers Squibb (07/24/25)
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  • Associate Principal Scientist

    Organon & Co. (Jersey City, NJ)
    …of biosimilar products. + Lead the development and implementation of global regulatory strategies by assessing CMC changes, identifying regulatory ... relevant functions to integrate new assets into Organon and lead regulatory sub-teams in both strategic and...alliance partners and commercial teams, in creating and implementing global regulatory CMC strategies for the registration,… more
    Organon & Co. (07/30/25)
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  • Senior Principal Scientist , Lead

    Bristol Myers Squibb (Princeton, NJ)
    …for assigned programs. Key responsibilities of this role are to act as a lead scientist to deliver and implement biomarker strategies for clinical programs, ... Medicine group + Represents Translational Medicine on cross-functional strategy and global project teams + Supports regulatory submissions, regulatory more
    Bristol Myers Squibb (06/01/25)
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  • Research Scientist

    Valvoline Global (Lexington, KY)
    …of automotive and industrial solutions. **How You'll Make an Impact** As a **Research Scientist ** this role will lead the development of Valvoline light duty ... **Why Valvoline Global Operations?** At **Valvoline Global Operations**...began; it's about where we're headed and how we'll lead the way. **We are originality in motion.** Our… more
    Valvoline Global (05/10/25)
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  • Scientist I

    Valvoline Global (Lexington, KY)
    **Why Valvoline Global Operations?** At **Valvoline Global Operations** , we're proud to be The Original Motor Oil, but we've never rested on being first. ... creating sustainable solutions for a better future. With a global presence, we develop future-ready products and provide best-in-class...began; it's about where we're headed and how we'll lead the way. We are originality in motion. Our… more
    Valvoline Global (07/24/25)
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  • Lead NLP Scientist - Consumer…

    JPMorgan Chase (Plano, TX)
    …impactful solutions-this is the team for you. As an Natural Language Processing Scientist within the Consumer Feedback Operations unit, you will play a pivotal role ... by utilizing machine learning models to detect complaints aligned with regulatory themes, investigating potential system, process, or policy issues. Additionally,… more
    JPMorgan Chase (06/15/25)
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  • Director, Safety Scientist

    BeOne Medicines (Emeryville, CA)
    Lead analysis of safety data and author relevant safety sections of global regulatory inquiries and periodic reports including Development Safety Update ... experience, including individual study design and filing plans. + Experienced in global regulatory requirements for pharmacovigilance. **Travel:** Less than 10%… more
    BeOne Medicines (07/02/25)
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  • Senior Manager, Oncology Early Stage Clinical…

    Pfizer (New York, NY)
    …Oncology Early Stage Clinical Scientist will work collaboratively with the Global Development Lead (and members of the development team) to establish, ... lead , coordinate, and execute the early oncology clinical development...other critical documents, eg, protocol amendments, investigator brochure, and regulatory documents. + Together with Clinical Operations, is responsible… more
    Pfizer (07/26/25)
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  • Sr. Scientist R&D Color Ingredients

    ADM (Erlanger, KY)
    …center located in Erlanger, Kentucky. We are looking for a highly motivated scientist to lead the color ingredient research. The successful candidate will ... delivery technologies. **Job purpose** In this role, the Sr Scientist will propose and lead color R&D...compliance with our stage gate project management process. + Lead the global color team. + Identify… more
    ADM (07/12/25)
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