• Associate Principal Clinical

    L'Oreal USA (Clark, NJ)
    …partners (CROs/external vendors, global Advanced Research, Applied Research, Safety and Regulatory Affairs , Technology Incubators, and skin and hair care ... Home (https://careers.loreal.com/en\_US/content/Home) / Job Search (https://careers.loreal.com/en\_US/jobs/SearchJobs) / 206467 Associate Principal Clinical Research Scientist, Open… more
    L'Oreal USA (06/11/25)
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  • Associate Director, Program Lead…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …Sankyo. The candidate will collaborate globally with Formulation and Analytical Scientists, Clinical Operations, Regulatory Affairs CMC, and Clinical ... to author the Dose Preparation Instructions and address questions from the clinical sites. The candidate will optimize and continuously improve the Pharmacy Manual… more
    Daiichi Sankyo Inc. (05/08/25)
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  • Regulatory Planning Manager (Hybrid)

    RWJBarnabas Health (Somerset, NJ)
    …should be in a closely related field such as health/business administration, regulatory compliance, accreditation or licensure associate , business development or ... Regulatory Planning Manager (Hybrid) - Somerset, NJReq #:0000170498.../ Management Status:Full-Time Shift:Day Facility:RWJBarnabas Health Corporate Services Department:External Affairs and Policy Salary:$91,472.00 - $129,204.00 per year Location:… more
    RWJBarnabas Health (06/11/25)
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  • GRA Device Lead, Associate Director

    Sanofi Group (Morristown, NJ)
    …within the Sanofi portfolio of products. The team is part of the Global Regulatory Affairs , Regulatory CMC and Device Department within Global Research ... **Job title** : GRA Device Lead ( Associate Director) **Location:** Cambridge. MA **,** Morristown, NJ...The incumbent will work closely with key stakeholders including clinical , medical affairs , Industrial Affairs more
    Sanofi Group (05/15/25)
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  • Director, Global Clinical

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …as an clinical /medical scientific consultant to health economic, medical affairs , marketing, regulatory , statistical and other research project team members, ... Development include the following: + Consults with patients or their representatives, clinical , regulatory , and scientific leaders and thoughtfully applies their… more
    Otsuka America Pharmaceutical Inc. (04/17/25)
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  • Executive Director, Product Development Team…

    Merck (Rahway, NJ)
    …with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development projects, and ... Scientist) has primary responsibility for the planning and directing of clinical research activities involving new or marketed medicines in the Atherosclerosis… more
    Merck (05/24/25)
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  • Associate Director, Global Regulator…

    Bristol Myers Squibb (Princeton, NJ)
    …(Masters, PhD, PharmD, BSN, etc.) with at least 3+ years of Regulatory Affairs experience in the pharmaceutical industry. **Key Competency Requirements** ... and in their personal lives. Read more: careers.bms.com/working-with-us . ** Associate Director, Global Regulatory Strategy, Neuroscience** **Position Summary:**… more
    Bristol Myers Squibb (06/05/25)
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  • Senior Director, Clinical Research,…

    Merck (Rahway, NJ)
    …with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development projects; and ... Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the… more
    Merck (05/24/25)
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  • Associate Director, Statistics - Eye Care

    AbbVie (Florham Park, NJ)
    …of work may include clinical trials, patient safety, and global medical affairs (GMA). The Associate Director works in partnership with experts in multiple ... development and drive alignment with functional management. Partner with other functions ( Clinical , Regulatory , Patient Safety, and GMA, etc.) to create… more
    AbbVie (05/14/25)
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  • Associate Director, Outcomes Research

    Merck (Rahway, NJ)
    …HTA submissions. The incumbent is expected to work cross-functionally with clinical development, medical affairs , biostatistics, market access, commercial and ... and barriers to reimbursement and market access, and provide input into clinical , regulatory , payer/access, marketing and evidence generation strategy and… more
    Merck (05/30/25)
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