• Executive Director , Global Program Lead…

    Bristol Myers Squibb (Princeton, NJ)
    …development and enable continuous improvements without compromising quality. + Engages senior leaders and functional area stakeholders to ensure alignment of program ... to develop program strategy and clinical program, commercialization strategy plans, business case development, and understands how access, pricing and reimbursement… more
    Bristol Myers Squibb (10/18/25)
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  • Associate Director , Small Molecule…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    **Associate Director , Small Molecule Analytical Development** + Lead and oversee phase appropriate method development and optimization for drug substance and drug ... with analytical team members, process chemistry, formulation development, regulatory affairs , quality assurance, and other departments to drive scientific… more
    Otsuka America Pharmaceutical Inc. (11/25/25)
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  • Associate Director , Global Regulator…

    Bristol Myers Squibb (Madison, NJ)
    …their personal lives. Read more: careers.bms.com/working-with-us . **Associate Director , Global Regulatory Strategy, Neuroscience** **Position Summary:** The ... BSN, etc.) with at least 3+ years of Regulatory Affairs experience in the pharmaceutical industry. **Key Competency Requirements**...and risks in written and verbal format to regulatory senior leadership team and other governing bodies. + Ability… more
    Bristol Myers Squibb (11/26/25)
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  • Director , RA Global Regulatory Strategy

    AbbVie (Florham Park, NJ)
    …YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Director , Regulatory Affairs Global Regulatory Strategy is responsible for ... of creative global strategies in line with applicable regulations to achieve business objectives for development and marketed products. When necessary, seeks expert… more
    AbbVie (09/20/25)
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  • Executive Director - Non-Clinical Safety…

    Organon & Co. (Jersey City, NJ)
    affairs , safety and pharmacovigilance, Chemistry, Manufacturing and Controls (CMC), medical affairs and business development are critical to the success of ... portfolio, including pipeline assets, life-cycle management of approved products, business development activities, and contributions to risk assessments and… more
    Organon & Co. (11/18/25)
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  • Director , Clinical Development

    J&J Family of Companies (Titusville, NJ)
    …CAPLYTA(R) Marketing team to support our growing impact in the marketplace. Director , Clinical Development, will be responsible for the leadership, oversight, and ... and clinical trial results at internal or external meetings. + Communicate to Senior Management and relevant functions any potential issues, risks or changes to the… more
    J&J Family of Companies (11/07/25)
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  • Senior Principal Scientist, Clinical…

    Merck (Rahway, NJ)
    …integrating state-of-the-art technology and applying rigorous scientific and ethical standards. The Senior Director ( Senior Principal Scientist) has primary ... to post-licensure). With a focus on late-stage development, the Senior Director will manage the entire cycle...further study of marketed compounds; and + Support of business development assessments of external opportunities. + Provide support… more
    Merck (11/19/25)
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  • Director , Therapy Education TMTT (Remote…

    Edwards Lifesciences (Newark, NJ)
    …changing work environment while demonstrating a sense of urgency + Conduct business and technical briefings for senior management + Regularly interacts ... of everything we do. As part of our Medical Affairs team, you'll foster internal and external collaboration to...treatment options. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of… more
    Edwards Lifesciences (11/19/25)
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  • Director , Global Labeling Strategy

    Otsuka America Pharmaceutical Inc. (Princeton, NJ)
    …efficient manner to meet required timelines. + Develop clear communications for senior management and SOP approvers to streamline and facilitate final label ... **Knowledge and skills** + Solid understanding of pharmaceutical regulatory affairs , global labeling regulatory requirements and industry practice. + Exceptional… more
    Otsuka America Pharmaceutical Inc. (11/19/25)
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  • Director , Intellectual Property

    Bausch Health (Bridgewater, NJ)
    …and optimizing costs associated with external counsel. + Collaborate with R&D, medical affairs , and other business stakeholders to identify and protect key ... innovations. + Collaborate with our business development teams to support IP diligence for new...personnel at all levels is required. Experience working with senior management/C-suite is preferred. The range of starting base… more
    Bausch Health (11/20/25)
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