• Director , Pharmaceutical Sciences Program…

    Takeda Pharmaceuticals (Boston, MA)
    …initiatives and may contribute to corporate, cross-divisional, and global initiatives **Accountabilities:** **Program Leadership** **:** + Provides strategic ... scientific leadership and program management for multiple global CMC development teams dealing with complex development programs that require scientific depth and… more
    Takeda Pharmaceuticals (06/27/25)
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  • Director , WW HEOR Hematology - Multiple…

    Bristol Myers Squibb (Madison, NJ)
    …asset level matrix teams, including Value Access, clinical development, medical affairs , regulatory, biostatistics to ensure full alignment and integration HEOR ... Team and Worldwide Brand Team + Develop and manage Global HEOR Book of Work to ensure optimal allocation...Work-life programs include paid national holidays and optional holidays, Global Shutdown Days between Christmas and New Year's holiday,… more
    Bristol Myers Squibb (09/21/25)
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  • Executive Medical Director , Clinical…

    AbbVie (North Chicago, IL)
    …opinion leader interactions related to the disease area(s); partners with Medical Affairs , Commercial and other functions in these activities as required, consistent ... the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those...bring out the best in others on a cross-functional global team. Must be able to lead and manage… more
    AbbVie (09/09/25)
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  • Medical Director , Clinical Development…

    AbbVie (North Chicago, IL)
    …opinion leader interactions related to the disease area(s); partners with Medical Affairs , Commercial and other functions in these activities as required, consistent ... the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those...bring out the best in others on a cross-functional global team. Must be able to lead through influence.… more
    AbbVie (08/13/25)
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  • Senior Scientific Director , Clinical…

    AbbVie (Irvine, CA)
    …opinion leader interactions related to the disease area(s); partners with Medical Affairs , Commercial and other functions in these activities as required, consistent ... the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those...bring out the best in others on a cross-functional global team. Must be able to lead through influence.… more
    AbbVie (08/08/25)
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  • Senior Director , Compound Development Team…

    J&J Family of Companies (Titusville, NJ)
    …leadership via matrix interactions includes individuals from TA strategy, GCSO, global regulatory affairs , project management, finance, legal, quality assurance, ... clinical research findings and presentations to relevant health authorities (eg global health authority meeting related to NDA/MAA/BLA) + Develop credible… more
    J&J Family of Companies (09/03/25)
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  • Sr. Director , Functional Service Provider…

    IQVIA (Durham, NC)
    …Clinical Data Management, Biostatistics, Medical Writing, Pharmacovigilance, and Regulatory Affairs . Establish and maintain relationships with senior levels within ... the job is located. \#DB-LI1 IQVIA is a leading global provider of clinical research services, commercial insights and...and welfare and/or other benefits. IQVIA is a leading global provider of clinical research services, commercial insights and… more
    IQVIA (08/19/25)
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  • Global Policy and Business Strategy…

    Bristol Myers Squibb (Princeton, NJ)
    …their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Director Global Policy and Business Strategy Integration is ... responsible for developing and implementing a Global Policy Strategy aligned with the business priorities with...role is accountable to ensure that Policy & Government Affairs insights are fully integrated into commercial business planning… more
    Bristol Myers Squibb (09/18/25)
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  • Director , Site Head of Quality Assurance

    Nitto Denko Corp. (Cincinnati, OH)
    …Head of Quality Assurance, you will report to the VP of Quality and Regulatory Affairs . The role is responsible for leading and managing all QA functions at the ... contribute to cross-functional decision-making. + Ensure site adherence to ICH, and global regulatory cGMP requirements (FDA, EMA, MHRA, etc.). + Maintain readiness… more
    Nitto Denko Corp. (09/15/25)
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  • Director of Quality Control

    Jabil (Hunt Valley, MD)
    …industries and a vast network of over 100 sites worldwide, Jabil combines global reach with local expertise to deliver both scalable and customized solutions. Our ... are maintained. + Collaborate with colleagues in Research & Development, Regulatory Affairs , Quality Assurance, and external partners and vendors or contractors to… more
    Jabil (09/11/25)
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