• Associate Manager - Regulatory

    Novo Nordisk (Plainsboro, NJ)
    …to make a difference? The Position We are seeking a dynamic and experienced Regulatory Affairs Labeling Associate Manager to oversee and lead critical tasks ... About the Department The Clinical , Medical and Regulatory (CMR) department...The ideal candidate will collaborate with cross-functional teams of Regulatory Affairs Therapeutic Area (TA) Managers, Global… more
    Novo Nordisk (01/25/25)
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  • Associate Director - Regulatory

    Novo Nordisk (Plainsboro, NJ)
    …Are you ready to make a difference? The Position The Associate Director, Regulatory Affairs - Advertising & Promotion will provide strategic regulatory ... Relationships Develop and maintain positive rapport and working relationships with Regulatory Affairs , Legal, Commercial, and other cross-functional stakeholders… more
    Novo Nordisk (01/22/25)
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  • Principal Scientist, Regulatory

    Merck (Rahway, NJ)
    …Development Teams and regulatory single point-of-contact for products within Global Regulatory Affairs and Clinical Safety (GRACS) and external to ... **Job Description** We are seeking a Director (Principal Scientist), Global Regulatory Affairs Liaison with a visionary, growth-oriented mindset that can help… more
    Merck (03/18/25)
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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 ...if:** + If you bring strong understanding of US FDA and international pharmaceutical guidance, regulations, drug development process,… more
    Regeneron Pharmaceuticals (03/12/25)
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  • Associate Director, Global Regulatory

    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 Director Regulatory

    Amneal Pharmaceuticals (Piscataway, NJ)
    …Global Regulatory Strategies: Formulate and lead global CMC and clinical regulatory strategies for Biologics, Biosimilars, and Small Molecules.Ensure ... advice to cross-functional teams and ensure compliance with FDA , EMA, and Health Canada regulations. Assess regulatory... FDA , EMA, and Health Canada regulations. Assess regulatory impact of changes in CMC procedures and oversee… more
    Amneal Pharmaceuticals (01/28/25)
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  • Director US Reg Affairs

    System One (Florham Park, NJ)
    Job Title: Director, US Regulatory Affairs Location: Florham Park, NJ (50% hybrid) Type: contract Overview: Support the Global Therapeutic Area Lead (GTAL), ... Regulatory Affairs (Senior Director) in developing and...a cross-functional team environment. + Strong knowledge of regional regulatory requirements and guidelines, including FDA regulations… more
    System One (03/06/25)
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  • Principal Scientist, Medical Affairs

    L'Oreal USA (Clark, NJ)
    …from all global R&I hubs in Advanced Research and other partners across clinical functions, regulatory , development labs, brand partners to ensure scientific ... programs to internal and external stakeholders on relevant projects and innovations. + Clinical Trial Support: Provide medical affairs support for clinical more
    L'Oreal USA (03/10/25)
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  • Principal Medical Science Liaison, US Medical…

    Gilead Sciences, Inc. (New Brunswick, NJ)
    …to requests for information, consistent with promotional compliance, PhRMA guidelines, and FDA regulatory requirements + Implements defined goals and objectives ... reporting to a Field Director. The MS will disseminate clinical information about Gilead's innovative hematology and oncology products...aligned with the Medical Affairs Plan of Action and other strategic initiatives +… more
    Gilead Sciences, Inc. (02/15/25)
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  • Biomedical Equipment Support Specialist

    Veterans Affairs, Veterans Health Administration (New York, NY)
    Summary The Biomedical Equipment Support Specialist provides clinical and administrative support to staff, patients, and administrators for all matters of concern ... throughout VA. Responsibilities The Biomedical Equipment Support Specialist provides clinical and administrative support to staff, patients, and administrators for… more
    Veterans Affairs, Veterans Health Administration (03/18/25)
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  • Senior Director - Training & Knowledge Management-…

    Novo Nordisk (Plainsboro, NJ)
    …in developing, implementing/facilitating, maintaining technical training programs related to GxP, Clinical , Medical and Regulatory affairs , Patient Safety ... About the Department The Clinical , Medical and Regulatory (CMR) department...the organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to providing… more
    Novo Nordisk (03/11/25)
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  • Associate Director, North America…

    J&J Family of Companies (Raritan, NJ)
    …and profoundly impact health for humanity. Learn more at https://www.jnj.com **Job Function:** Regulatory Affairs Group **Job Sub** **Function:** Regulatory ... industry, consumer industry or health authority regulated industry + At least 3 years of Regulatory Affairs experience required with focus on the NA region and … more
    J&J Family of Companies (03/19/25)
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  • Senior Director, Global Regulatory

    Sanofi Group (Bridgewater, NJ)
    …of US Regulatory strategies (eg, submissions, product defense, labeling development, FDA enforcement, clinical trial support, FDA contacts). + Provide ... you will be the primary therapeutic area liaison with FDA 's Office of Prescription Drug Promotion (OPDP) for drugs,...started? **Main Responsibilities** + In conjunction with the Global Regulatory Affairs Head of Global Advertising &… more
    Sanofi Group (02/04/25)
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  • Senior Director, Clinical Leader…

    J&J Family of Companies (Raritan, NJ)
    …quality monitoring & compliance, clinical supplies unit, TA strategy, regulatory affairs , data management, medical writing, biostatistics, global medical ... clinical team in responding to medical and compound-related issues + Working with Regulatory Affairs and global clinical operations with regard to… more
    J&J Family of Companies (03/04/25)
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  • Medical Director - Clinical Development…

    Novo Nordisk (Plainsboro, NJ)
    …include working with Headquarters, NA CMR including Clinical Trial Management, Medical Affairs , Regulatory Affairs and other NNI skill areas. External ... About the Department The Clinical , Medical and Regulatory (CMR) department...the organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to providing… more
    Novo Nordisk (03/04/25)
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  • Director, Clinical Pharmacology

    Bausch Health (Edison, NJ)
    …Management, CMC, Analytical Sciences, Nonclinical, Clinical Operations, Clinical /Medical Affairs , Biostatistics, and Regulatory Affairs . + Lead the ... Responsible for the technical content and timely completion of clinical pharmacology deliverables as well as regulatory ...dermatology drugs is preferred. + Track record of successful regulatory agency (US FDA ) submissions and interactions… more
    Bausch Health (03/20/25)
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  • Clinical Program Manager

    Danaher Corporation (New York, NY)
    …within medical device (IVD preferred), biotech, or pharmaceutical + Working knowledge of FDA regulatory requirements related to clinical research + Strong ... and mentorship to Clinical Operations staff.This position is part of the Clinical Affairs department and will be Remote.In this role, you will have… more
    Danaher Corporation (03/07/25)
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  • Associate Principal Scientist, Clinical

    Merck (Rahway, NJ)
    …subject matter expert in flow cytometry, working with project teams, biomarker leaders, clinical operations, regulatory affairs , and physicians to implement ... datasets. + ** Regulatory Knowledge:** Understanding of regulatory guidelines ( FDA , EMA) pertaining to biomarker development and clinical trial processes.… more
    Merck (03/14/25)
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  • Lead Data Scientist - Clinical Data…

    Novo Nordisk (Plainsboro, NJ)
    About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and… more
    Novo Nordisk (03/19/25)
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  • Medical Director, Endocrine Medical Sciences (US…

    Ascendis Pharma (Princeton, NJ)
    …programs, competitive landscape, new therapies, clinical trends, and newly issued regulatory rules and FDA guidance to promptly identify any potential impact ... advocacy groups. + Work with internal stakeholders including Commercial, Legal, Regulatory , Clinical Development, Clinical Operations, Compliance,… more
    Ascendis Pharma (03/11/25)
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