• 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 , 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 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 (10/19/24)
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  • Regulatory Affairs Clinical FDA…

    Amneal Pharmaceuticals (Piscataway, NJ)
    …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 managing, coordinating, tracking and follow-up on FDA Communications and ANDA status for assigned… more
    Amneal Pharmaceuticals (11/14/24)
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  • Political Affairs & Governance Manager

    PSEG (Newark, NJ)
    …well as the attention, camaraderie and care for one another you might typically associate with a small business. Our focus on combatting climate change through clean ... political and lobbying activities of federal and state government affairs and other CC departments as needed. This role...including setting Board meeting agendas, working with the PEGPAC director to create the PEGPAC budget and manage all… more
    PSEG (01/07/25)
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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 Launch Excellence

    Teva Pharmaceuticals (Parsippany, NJ)
    Associate Director Launch Excellence Date: Dec 23, 2024 Location: Parsippany, United States, New Jersey, 07054 Company: Teva Pharmaceuticals Job Id: 59927 **Who ... making a difference, and new people to make a difference with. **The opportunity** The Associate Director , Launch Excellence will report to the Sr Director more
    Teva Pharmaceuticals (12/24/24)
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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 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 , 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 - Product…

    Merck (Rahway, NJ)
    …and systems for a pharmaceutical company, ensuring compliance with regulatory requirements and maintaining high-quality standards. Product managers must possess ... cross-functional teams to develop and implement pharmacovigilance strategies that meet regulatory requirements and ensure patient safety, quality and compliance. +… more
    Merck (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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  • 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 ... create breakthrough science that radically changes the way we approach serious diseases. The Director will report to an Associate Vice President in the Oncology… more
    Merck (01/16/25)
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  • Executive Director , Global Pharma…

    Merck (Rahway, NJ)
    **Job Description** The Executive Director , Global Pharma Communications is responsible for leading, developing and executing US and global communications strategies ... infectious diseases, neuroscience, ophthalmology, and immunology. Reporting to the Associate Vice President, Human Health and Manufacturing Communications, the… more
    Merck (01/14/25)
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  • Associate General Counsel, Market Access…

    Teva Pharmaceuticals (Parsippany, NJ)
    …and new people to make a difference with. **The opportunity** The Senior Director , Associate General Counsel, Market Access and Pricing role reports directly ... Associate General Counsel, Market Access & Pricing Date:...US, as well as providing legal support to Government Affairs and Payor Marketing. This role partners principally with… more
    Teva Pharmaceuticals (01/10/25)
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  • Associate General Counsel, Transactions

    Teva Pharmaceuticals (Parsippany, NJ)
    …people to make a difference with. **The opportunity** The Sr. Director , Associate General Counsel, Transactions & Corporate Affairs role reports directly to ... Associate General Counsel, Transactions Date: Jan 6, 2025...functions, including R&D, intellectual property, supply chain, finance, and regulatory affairs . This role will also help… more
    Teva Pharmaceuticals (12/12/24)
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  • Distinguished Scientist, Product Development Team…

    Merck (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
    Merck (12/19/24)
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