• 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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  • Merck & Co. (Rahway, NJ)
    …--Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... breakthrough science that radically changes the way we approach serious diseases. --The Director will report to an Associate Vice President in the Oncology… more
    HireLifeScience (01/16/25)
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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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  • Merck & Co. (Rahway, NJ)
    …a cross-functional Senior/ Executive Director group of experts in commercialization, regulatory affairs , statistics, medical affairs and manufacturing to ... teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs and new indications for existing products. We… more
    HireLifeScience (01/25/25)
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  • Merck & Co. (Rahway, NJ)
    …studies.Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication.Specifically, The Clinical Director May Be… more
    HireLifeScience (01/15/25)
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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 (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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  • Associate Director Regulatory

    Amneal Pharmaceuticals (Piscataway, NJ)
    …and company goals and objectives. Essential Functions: + Develop and Execute Global Regulatory Strategies: Formulate and lead global CMC and clinical regulatory ... strategies for Biologics, Biosimilars, and Small Molecules.Ensure alignment with regulatory trends, innovation, and compliance while balancing business benefits and… more
    Amneal Pharmaceuticals (01/28/25)
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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 , Therapeutic…

    Bristol Myers Squibb (Summit, 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 (01/28/25)
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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 of Compliance…

    CUNY (Bronx, NY)
    Associate Director of Compliance and Diversity **POSITION DETAILS** Hostos Community College is seeking to fill the position of Associate Director of ... interviews and other evidence that has been gathered. The Associate Director of Compliance and Diversity will...Human Resources Department, Dean of Students Office, and Legal Affairs Office to ensure compliance with EEO, OFCCP and… more
    CUNY (01/28/25)
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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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