• Director , Scientific

    The Coca-Cola Company (Whitestone, NY)
    …relevant science discipline required. **Job Description Summary** : The Director , Scientific and Regulatory Affairs Compliance and Innovation develops, ... improves, and drives compliance to all Regulatory requirements at BODYARMOR. In addition, this role also...5 to 7 years of experience in a similar Regulatory role, food and beverage experience preferred. + … more
    The Coca-Cola Company (01/25/25)
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  • Medical/ Scientific Director

    AbbVie (Florham Park, NJ)
    …strategy. + Must possess excellent oral and written English communication skills. Scientific Director Qualifications: + Advanced Degree PhD or PharmD. Additional ... scientific strategic and operational input into core medical affairs activities such as: healthcare professional/provider interactions (HCPs, Patients and… more
    AbbVie (12/19/24)
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  • Associate Medical/ Scientific

    AbbVie (Florham Park, NJ)
    …including regulatory guidelines to meet customer needs. Qualifications Associate Scientific Director Qualifications + Bachelor's Degree in the sciences. ... level will be determined by the qualifications listed below. Purpose The Associate Scientific Director provides medical and scientific strategic and… more
    AbbVie (01/18/25)
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  • Director , Global Regulatory

    Merck (Rahway, NJ)
    …(engineering or scientific discipline, MBA) + Knowledge of Global Regulatory Affairs and Clinical Safety organization, roles, and responsibilities. Current ... **Job Description** The Global Regulatory Affairs and Clinical Safety Global Process Lead is responsible for overseeing and managing Global Regulatory more
    Merck (01/10/25)
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  • Senior Director , US Regulatory

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …be responsible for bringing the issue and potential solutions to the Head of US Regulatory Affairs in conjunction with the assigned US RA strategist on the ... science and technology. With more than 125 years of scientific expertise and a presence in more than 20...transparent ways of working across the Alliance within US regulatory affairs and will work closely with… more
    Daiichi Sankyo Inc. (11/13/24)
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  • Principal Scientist/ Director

    Merck (Rahway, NJ)
    …Drug-Device Combinations CMC (Chemistry, Manufacturing & Controls), you will report to the Director of Device Regulatory Affairs for Autoinjector Development ... Support device design control activities and documentation reviews + Provide evaluations of regulatory state of affairs of any devices and combination products,… more
    Merck (01/14/25)
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  • Associate Director , Regulatory

    Gilead Sciences, Inc. (Parsippany, NJ)
    …Advertising and Promotion (RA Ad/Promo) is a core function within Gilead's Global Regulatory Affairs organization and acts as a critical strategic partner across ... critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as...Experience working with external contractors supporting the work of regulatory affairs is a plus. + Experience… more
    Gilead Sciences, Inc. (11/16/24)
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  • Director Global Regulatory

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …More Years of relevant pharmaceutical experience including 5 years of experience within Regulatory Affairs + Knowledge of IND, NDA/BLA submission experience + ... by leveraging our world-class science and technology. With more than 125 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and… more
    Daiichi Sankyo Inc. (12/18/24)
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  • Associate Director , Regulatory

    Bristol Myers Squibb (Madison, NJ)
    …years in the industry with at least 4+ years of US Medical Device Regulatory Affairs experience **Key Competencies** + Experience in successfully leading teams; ... careers.bms.com/working-with-us . **Position Responsibilities** + Leadership responsibility for global regulatory strategy to support the development of biomarkers, companion… more
    Bristol Myers Squibb (01/03/25)
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  • Director , US Regulatory

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …or More Years in the pharmaceutical industry required. + 8 or More Years in regulatory affairs + Experience in providing regulatory strategic input into the ... science and technology. With more than 100 years of scientific expertise and a presence in more than 20...with FDA. This role will create and implement effective regulatory strategies to deliver on efficient and robust development… more
    Daiichi Sankyo Inc. (12/01/24)
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  • Director , US Regulatory

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …+ 7 or More Years in the pharmaceutical industry + 4 or More Years in regulatory affairs , NDA, sNDA, BLA filing to FDA **Travel** Ability to travel up to ... science and technology. With more than 100 years of scientific expertise and a presence in more than 20...FDA; direct, coordinate and implement the preparation of all regulatory submissions and provide regulatory support across… more
    Daiichi Sankyo Inc. (11/09/24)
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  • Director , US Regulatory

    Insight Global (Basking Ridge, NJ)
    …. Skills and Requirements 10+ years in the pharmaceutical industry. 8+ years in regulatory affairs . Experience in providing regulatory strategic input into ... and partnering with FDA. This role will create and implement effective regulatory strategies to deliver on efficient and robust development plans. The individual… more
    Insight Global (01/25/25)
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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 ... science and technology. With more than 100 years of scientific expertise and a presence in more than 20...serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational… more
    Daiichi Sankyo Inc. (01/18/25)
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  • Deputy Executive Director , External…

    City of New York (New York, NY)
    …Mayor's Office of Community Mental Health (OCMH) is seeking a Deputy Executive Director , External Affairs who will head the multidisciplinary External Affairs ... Director of OCMH and will directly manage 4 staff members.The Deputy Executive Director , External Affairs will work closely with the Executive Director more
    City of New York (12/07/24)
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  • Director , US Medical Affairs

    Bristol Myers Squibb (Madison, NJ)
    …and in their personal lives. Read more: careers.bms.com/working-with-us . The Medical Director , US Medical, Multiple Myeloma will report to the Senior Director ... the US Commercialization organization, WW Medical, Clinical Research and Development, Regulatory , Translational Development, and Market Access, and will lead the US… more
    Bristol Myers Squibb (01/22/25)
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  • US Medical Director - Portfolio, New…

    Sanofi Group (Morristown, NJ)
    …on millions of patients around the world. **Main Responsibilities:** The US Medical Director - New Products will provide medical and scientific guidance for the ... **Job Title:** US Medical Director - Portfolio, New Products, Innovation- Vaccines **Location** :...of Medical leaders who are a trusted source of scientific and medical information and shared insights; effective and… more
    Sanofi Group (11/22/24)
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  • US Medical Director , Mainline Vaccines

    Sanofi Group (Morristown, NJ)
    **Job Title:** US Medical Director , Mainline Vaccines **Location** : Bridgewater, NJ / Morristown, NJ **About the Job** The North American Medical Team at Sanofi is ... high-performing team of Medical leaders who are a trusted source of scientific and medical information and shared insights; effective and innovative strategic… more
    Sanofi Group (11/18/24)
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  • Clinical Director , Oncology Early…

    Merck (Rahway, NJ)
    …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Director may… more
    Merck (01/16/25)
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  • Director , Labeling

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …rare diseases and immune disorders. **Summary** This position serves as the Global Regulatory Affairs (GRA) Labeling Strategy expert to the Global Product Team ... science and technology. With more than 100 years of scientific expertise and a presence in more than 20...for cross-functional teams on RA labeling issues. Collaborate with Regulatory Affairs and Labeling colleagues in other… more
    Daiichi Sankyo Inc. (01/22/25)
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  • VP, Medical Director

    Cline Davis & Mann (New York, NY)
    **Overview** The VP, Medical Director is responsible for leading the agency team in the understanding and application of scientific /clinical account data. A high ... is required. He/she, in collaboration with his/her team, will prepare scientific and strategic analyses of data, conduct research and disseminate brand/category… more
    Cline Davis & Mann (12/20/24)
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