• Daiichi Sankyo, Inc. (Bernards, NJ)
    …well as other research areas centered around rare diseases and immune disorders. Summary: The Associate Director , Regulatory Affairs - Regulatory ... provides planning and drives coordination of global and US regulatory activities. The Associate Director ...provides impactful contributions to the RPM group and the regulatory affairs organization by identifying gaps in… more
    HireLifeScience (01/06/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …Years pharmaceutical industry experience required4 or More Years of direct regulatory affairs experience, including US labeling experience requiredExperience ... This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational leadership on product… more
    HireLifeScience (01/06/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …or More Years in the pharmaceutical industry preferred1 or More Years in regulatory affairs requiredExperience in (s)NDA/BLA filing to FDA preferred Travel ... with FDA. This role will create and implement effective regulatory strategies to deliver on efficient and robust development...will direct, coordinate and implement the preparation of US regulatory submissions and provide US regulatory support… more
    HireLifeScience (12/19/24)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …other research areas centered around rare diseases and immune disorders.Summary: The Associate Director , Regional Marketing Conventions & Field Programs will be ... and more, while ensuring adherence to DS policies and procedures. The Associate Director , Regional Marketing Conventions & Field Programs is responsible… more
    HireLifeScience (01/01/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …to Clinical Operations, Clinical Development, Biostatistics and Data Management, Regulatory Affairs , Quantitative Clinical Pharmacology, Clinical Safety and ... Pharmacovigilance, Regulatory /Risk Management, Quality Assurance, Medical Affairs , Translational Research, Research, Informatics Services, Project Management and… more
    HireLifeScience (12/13/24)
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  • Associate Director

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …well as other research areas centered around rare diseases and immune disorders. **Summary:** The Associate Director , Regulatory Affairs - Regulatory ... provides planning and drives coordination of global and US regulatory activities. The Associate Director ...provides impactful contributions to the RPM group and the regulatory affairs organization by identifying gaps in… more
    Daiichi Sankyo Inc. (01/07/25)
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  • Associate Director , US…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …More Years in the pharmaceutical industry preferred + 1 or More Years in regulatory affairs required + Experience in (s)NDA/BLA filing to FDA preferred ... with FDA. This role will create and implement effective regulatory strategies to deliver on efficient and robust development...will direct, coordinate and implement the preparation of US regulatory submissions and provide US regulatory support… more
    Daiichi Sankyo Inc. (12/18/24)
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  • Associate Director , Global…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …pharmaceutical industry experience required + 4 or More Years of direct regulatory affairs experience, including US labeling experience required + Experience ... This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational leadership on product… more
    Daiichi Sankyo Inc. (10/19/24)
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  • Associate Director , Global Oncology…

    Sanofi Group (Bridgewater, NJ)
    **Job title** : Associate Director , Global Oncology Corporate Communications **Location:** Cambridge, MA 50% remote working; limited travel expected. **About the ... the world. Sanofi is looking for a proactive, high-energy Associate Director to join the Global Specialty...global communications programming in support of clinical data and regulatory milestones as well as pipeline; 2) supporting development… more
    Sanofi Group (12/19/24)
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  • Associate Director , Regional…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …research areas centered around rare diseases and immune disorders. **Summary:** The Associate Director , Regional Marketing Conventions & Field Programs will be ... and more, while ensuring adherence to DS policies and procedures. The Associate Director , Regional Marketing Conventions & Field Programs is responsible… more
    Daiichi Sankyo Inc. (11/23/24)
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  • Associate Director , Consumer…

    Sanofi Group (Bridgewater, NJ)
    **Job Title:** Associate Director , Consumer Marketing - US Rare Hematology **Location** : Cambridge, MA **_About the Job_** This role will drive consumer ... disorder. This position is based in Cambridge, MA and will report into Director of Consumer marketing for rare hematology. We are an innovative global healthcare… more
    Sanofi Group (12/03/24)
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  • Associate Director , Technical Lead,…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …to Clinical Operations, Clinical Development, Biostatistics and Data Management, Regulatory Affairs , Quantitative Clinical Pharmacology, Clinical Safety and ... Pharmacovigilance, Regulatory /Risk Management, Quality Assurance, Medical Affairs , Translational Research, Research, Informatics Services, Project Management and… more
    Daiichi Sankyo Inc. (12/13/24)
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  • Associate Director , Medical…

    J&J Family of Companies (Titusville, NJ)
    This position will report to the Director , Medical Information Scientific Engagement (MISE) and will have responsibility for providing direct oversight of the ... Essential Functions: + Serves as a strategic partner with internal Scientific Affairs colleagues to find opportunities for outstanding service delivery and leads all… more
    J&J Family of Companies (01/07/25)
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  • Associate Medical Director /Medical…

    AbbVie (Branchburg, NJ)
    …Key Stakeholders: PST Lead, Search and Evaluation Team, Project Management, Regulatory Affairs , Discovery, Clinical Operations Additional Information Applicable ... or Development Safety Update Report) for early development assets *Apply current regulatory guidance as appropriate for safety surveillance and authorship of PV… more
    AbbVie (11/20/24)
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