• Associate Director

    Taiho Oncology (Princeton, NJ)
    Associate Director , Regulatory Affairs Strategy Princeton, NJ, USA Req #415 Wednesday, November 27, 2024 Looking for a chance to make a meaningful ... filing in US and Europe. Position Summary: + Under the direction of regulatory affairs management, the incumbent independently prepares and directs global … more
    Taiho Oncology (11/28/24)
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  • Associate Director

    Novo Nordisk (Plainsboro, NJ)
    …changing lives for a living. Are you ready to make a difference? The Position The Associate Director , Regulatory Affairs - Advertising & Promotion will ... strong and positive working relationship with OPDP reviewers. Report to Senior Director , Regulatory Affairs - Advertising & Promotion. Essential Functions +… more
    Novo Nordisk (01/22/25)
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  • Associate Director

    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 ... + Experience working with external contractors supporting the work of regulatory affairs is a plus. + Experience authoring and/or implementing processes. +… more
    Gilead Sciences, Inc. (11/16/24)
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  • Associate Director

    Bristol Myers Squibb (Princeton, 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 (01/22/25)
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  • Associate Director

    IQVIA (Parsippany, NJ)
    regulatory document types; * May plan and deliver workshops or presentations on Regulatory Affairs topics for conferences or publications; * May be assigned ... Job Overview Direct, oversee and manage complex regulatory projects, ensuring quality deliverables on time and within budget. Ensure that all project work is… more
    IQVIA (01/24/25)
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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 ... 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. (01/18/25)
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  • Associate Medical/Scientific…

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

    Scotiabank (New York, NY)
    Associate Director , Legal Counsel, Legal and Corporate Affairs **Requisition ID:** 206757 **Salary Range:** 180,000.00 - 211,800.00 _Please note that the ... advising the front office and other internal stakeholders on legal and regulatory matters related to the business. + Independently draft and/or assist the… more
    Scotiabank (01/02/25)
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  • Associate Director , Global…

    Takeda Pharmaceuticals (Trenton, NJ)
    …company that will inspire you and empower you to shine? Join us as an Associate Director , Global Regulatory Project Management and Strategic Planning - ... Neuroscience TAU within our Global Regulatory Affairs organization, based remotely. + Partners with the Global Regulatory Lead (GRL) on Global Regulatory more
    Takeda Pharmaceuticals (01/19/25)
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  • Associate Director

    Takeda Pharmaceuticals (Trenton, NJ)
    …innovative opportunities to improve processes and infrastructure in line with global regulatory expectations and Global Regulatory Affairs (GRA) technology ... goals. + Demonstrates leadership and a deep understanding of global regulatory affairs (GRA) information/data regulations and guidelines, proactively addressing… more
    Takeda Pharmaceuticals (01/24/25)
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  • Associate Director , RA Submissions

    J&J Family of Companies (Raritan, NJ)
    Johnson & Johnson Innovative Medicine is recruiting for Associate Director , RA Submissions. The position can be located on-site/hybrid in the US (Titusville, NJ; ... Bachelor's degree or equivalent experience in a related field (Pharmacy, Life Sciences, Regulatory Affairs , etc.) + A minimum of 8 years of experience in … more
    J&J Family of Companies (01/10/25)
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  • Associate Director , Therapeutic…

    Bristol Myers Squibb (New Brunswick, NJ)
    …in their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Associate Director , Therapeutic Area Audit Strategy Lead will be ... Oversee study centers, countries, investigators and connect with PV, Medical Affairs and Regulatory Affairs + Contribute to develop Quality Management… more
    Bristol Myers Squibb (01/25/25)
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  • Associate Director , Solutions…

    Sanofi Group (Bridgewater, NJ)
    **Job Title:** Associate Director , Solutions and Industry Partnerships -Vaccines **Location:** Remote **About the Job** As the Associate Director , ... designed for specific partnership channels + Work closely with HS Solutions, Public Affairs , HIT Solutions, Brand Marketing, and Market Access to ensure content both… more
    Sanofi Group (01/23/25)
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  • Associate Director , Clinical Data…

    Merck (Rahway, NJ)
    **Job Description** **Job Overview:** We are seeking a highly qualified and experienced Associate Director in Data Management to lead our data management team in ... stakeholders such as , Clinical Research Associates, Statisticians, Quality Assurance, and Regulatory Affairs to drive data excellence and enhance the efficiency… more
    Merck (01/15/25)
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  • Associate Director , Global Labeling…

    Takeda Pharmaceuticals (Trenton, NJ)
    …in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be responsible for ... and assures that Takeda labeling content and processes conform to regulatory requirements. Management of Local Exceptions and LOC Interactions + Manages… more
    Takeda Pharmaceuticals (01/15/25)
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  • Associate Director , Biostatistics…

    Mitsubishi Chemical Group (Jersey City, NJ)
    …on real-world evidence, and creating hope for all facing illness. The Associate Director , Biostatistics is responsible for providing statistical support to ... 2022. The company handles research, clinical development, sales, marketing, medical affairs , supply chain,and business development functions. MTPA is dedicated to… more
    Mitsubishi Chemical Group (11/14/24)
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  • Associate Director , Quality…

    Mitsubishi Chemical Group (Jersey City, NJ)
    …on real-world evidence, and creating hope for all facing illness. The Associate Director , Quality Management System will be responsible for supporting ... 2022. The company handles research, clinical development, sales, marketing, medical affairs , supply chain,and business development functions. MTPA is dedicated to… more
    Mitsubishi Chemical Group (01/16/25)
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  • Associate Director , Statistical…

    Mitsubishi Chemical Group (Jersey City, NJ)
    …on real-world evidence, and creating hope for all facing illness. The Associate Director , Statistical Programming is responsible for building and maintaining ... 2022. The company handles research, clinical development, sales, marketing, medical affairs , supply chain,and business development functions. MTPA is dedicated to… more
    Mitsubishi Chemical Group (11/14/24)
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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 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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