• Director , Regulatory Affairs

    Mitsubishi Chemical Group (Jersey City, NJ)
    …researching on real-world evidence, and creating hope for all facing illness. The Director , Regulatory Affairs provides strategic global regulatory ... unmet medical needs in North American markets. In the United States , MTPA launched rare diseases treatments...requests, and briefing documents. + Acts as liaison between Regulatory Affairs and other functional areas, including… more
    Mitsubishi Chemical Group (10/18/24)
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  • Director , Regulatory Affairs

    Regeneron Pharmaceuticals (Basking Ridge, NJ)
    The Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus on ... Clinical Regulatory filings and provide regulatory leadership on...you if:** + If you bring strong understanding of US FDA and international pharmaceutical guidance, regulations, drug development… more
    Regeneron Pharmaceuticals (12/11/24)
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  • Director , Regulatory Affairs

    Merck (Rahway, NJ)
    **Job Description** The Regulatory Affairs Headquarters Principal Scientist is responsible for development and implementation of global regulatory strategy ... point of contact on those projects within Global Regulatory Affairs and Clinical Safety (GRACS) and...in certain states and cities within the United States . Final determinations with respect to… more
    Merck (12/04/24)
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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 ... objectives. This group also represents Gilead's commercial activities to US regulatory agencies. You will manage the...conditions of the applicable plans. **For jobs in the United States :** As an equal opportunity employer,… more
    Gilead Sciences, Inc. (11/16/24)
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  • Associate Director , Regulatory

    Bristol Myers Squibb (Madison, NJ)
    …BSN, etc.) with 5 years in the industry with at least 4+ years of US Medical Device Regulatory Affairs experience **Key Competencies** + Experience in ... **Working with Us ** Challenging. Meaningful. Life-changing. Those aren't words that... . **Position Responsibilities** + Leadership responsibility for global regulatory strategy to support the development of biomarkers, companion… more
    Bristol Myers Squibb (12/25/24)
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  • Senior Director , US

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …leader will be responsible for bringing the issue and potential solutions to the Head of US Regulatory Affairs in conjunction with the assigned US RA ... accountable for ensuring consistent and transparent ways of working across the Alliance within US regulatory affairs and will work closely with the US more
    Daiichi Sankyo Inc. (11/13/24)
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  • Director , US Regulatory

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …robust development plans. The individual will direct, coordinate and implement the preparation of US regulatory submissions and provide US regulatory ... growth, thereby accomplishing corporate goals. **Responsibilities:** + Develop and implement US regulatory strategy for assigned project(s). Strategize and plan… more
    Daiichi Sankyo Inc. (12/01/24)
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  • Associate Director , US

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …robust development plans. The individual will direct, coordinate and implement the preparation of US regulatory submissions and provide US regulatory ... growth, thereby accomplishing corporate goals. **Responsibilities** + Develop and implement US regulatory strategy for assigned project(s). + Strategize and… more
    Daiichi Sankyo Inc. (12/18/24)
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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 ... and partner with FDA; direct, coordinate and implement the preparation of all regulatory submissions and provide regulatory support across all global projects,… more
    Daiichi Sankyo Inc. (11/09/24)
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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 + ... and immune disorders. **Summary:** Responsible for leading and developing global regulatory strategy for assigned development projects. Represents Daiichi Sankyo's … more
    Daiichi Sankyo Inc. (12/18/24)
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  • Associate Director , Global…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …More Years pharmaceutical industry experience required + 4 or More Years of direct regulatory affairs experience, including US labeling experience required + ... US or EU. Preparation of updated Core Data Sheets, and EU and US Documentation: Independently manages, prepares and implements regulatory documents (eg, USPI,… more
    Daiichi Sankyo Inc. (10/19/24)
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  • Regulatory Affairs Clinical FDA…

    Amneal Pharmaceuticals (Piscataway, NJ)
    Description: The Associate II (A), assists with minimal guidance, the Senior Director of Regulatory Affairs Clinical/ FDA Communications.Assists the Senior ... Director of Regulatory Affairs / Clinical Affairs in...Audits conducted by the CRA ANDA Department within the US and International. + Submission/tracking of inter department communications… more
    Amneal Pharmaceuticals (11/14/24)
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  • Senior Legislative Officer

    NJEDA (Newark, NJ)
    …Staff, Managing Director - Policy, Research, and Government Affairs , and Director - Legislative & Regulatory Affairs to develop positions and ... contributes to bill comments prepared by the Legislative & Regulatory Affairs team on proposed legislation that...Selected candidates must be authorized to work in the United States per the Department of Homeland… more
    NJEDA (12/24/24)
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  • Accreditation Specialist;(RN) Mount Sinai Health…

    Mount Sinai Health System (New York, NY)
    …of CMO - MSH, Mount Sinai Hospital **Responsibilities** In collaboration with Senior Director of Regulatory Affairs , and other system leadership, directs ... **Job Description** A member of MSHS regulatory team, the Accreditation Specialist is a key...trends, practices, and developments. Other duties as assigned. **About Us ** **Strength Through Diversity** The Mount Sinai Health System… more
    Mount Sinai Health System (09/30/24)
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  • Director US Medical Affairs

    Bayer (Whippany, NJ)
    …of brilliant and diverse minds to make a real difference, there's only one choice.** ** Director US Medical Affairs Women's Healthcare** The Director ... TASKS AND RESPONSIBILITIES** The primary responsibilities of this role, Director US Medical Affairs Women's...contact information below. Bayer is an E-Verify Employer. **Location:** United States : Connecticut : Residence Based… more
    Bayer (12/20/24)
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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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  • Associate Director , US Medical…

    Bristol Myers Squibb (Madison, NJ)
    …their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with- us . The Associate Director , US Medical, Multiple Myeloma ... will report to the Director , US Medical Multiple Myeloma Asset Lead. He/she will be...**Key Responsibilities** + Support development and execution of the US Medical Affairs plans, in coordination with… more
    Bristol Myers Squibb (12/23/24)
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  • Medical Director /Scientific…

    AbbVie (Florham Park, NJ)
    …our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and ... medical and scientific strategic and operational input into core medical affairs activities such as: health-care professional and provider interactions; generation… more
    AbbVie (12/26/24)
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  • Medical/Scientific Director , Medical…

    AbbVie (Florham Park, NJ)
    …our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and ... and 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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  • Addiction Section Chief and Opiate Treatment…

    Veterans Affairs, Veterans Health Administration (Bronx, NY)
    …are deemed to have met the basic requirements of the occupation. Basic Requirements: United States Citizenship: Non-citizens may only be appointed when it is not ... a Full-Time Addiction Section Chief and Opiate Treatment Program Director . The Board Certified applicant should possess the leadership,...surgery in a State, Territory, or Commonwealth of the United States , or in the District of… more
    Veterans Affairs, Veterans Health Administration (10/18/24)
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