• 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 ( Early Development) provides strategic ... in the rare disease space. In this role, the Director defines and implements regulatory strategies; works...requests, and briefing documents. + Acts as liaison between Regulatory Affairs and other functional areas, including… more
    Mitsubishi Chemical Group (06/21/24)
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  • Senior Director , Regulatory

    Mitsubishi Chemical Group (Jersey City, NJ)
    …real-world evidence, and creating hope for all facing illness. The Senior Director , Regulatory Affairs - Clinical ( Early Development), may be called upon ... to facilitate timely drug development and registration. The Senior Director , Regulatory Affairs - Clinical...+ procedural cross-functional teams. + Assigns reports to represent early - and late-stage project teams and ensures timely and… more
    Mitsubishi Chemical Group (06/21/24)
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  • Director Regulatory Affairs

    Merck (Rahway, NJ)
    …and solutions to the world. **Looking for someone with a growth mindset. The Director , Regulatory Affairs Liaison is responsible for:** + Developing ... **Job Description** Our Regulatory Affairs team bring new medical...committee charters. (Therapeutic area document review committees (DRC), Global Regulatory Team (GRT) Product Development Team (PDT), Early more
    Merck (07/22/24)
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  • Director , Regulatory Affairs

    Merck (Rahway, NJ)
    **Job Description** **Position Title** - Principal Scientist **Department** - Global Regulatory Affairs and Clinical Safety - Vaccine & Infectious Disease ... **Brief Description of Position** The Regulatory Affairs Headquarters Principal Scientist is responsible for development and implementation of global … more
    Merck (08/08/24)
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  • Senior Director Regulatory

    Merck (Rahway, NJ)
    **Job Description** Our Regulatory Affairs team bring new medical advancements to the world by facilitating communications and procedures that allow swift, ... someone with a growth mindset. **Position Description:** The Senior Director , Global Regulatory Lead, is responsible for... regulatory single point-of-contact for products within Global Regulatory Affairs and Clinical Safety (GRACS) and… more
    Merck (07/06/24)
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  • Director , Regulatory Affairs

    Gilead Sciences, Inc. (Parsippany, NJ)
    …within the Inflammation TA. You will work closely with the Inflammation Fibrosis Regulatory Affairs (RA) Franchise Lead, Regional Regulatory Liaisons and ... be accountable for the development and execution of global regulatory strategies for early and late-stage assets...regulatory strategy. + Provide strategic guidance as the Regulatory Affairs Inflammation subject matter expert on… more
    Gilead Sciences, Inc. (08/10/24)
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  • Scientific Director /Senior Scientific…

    AbbVie (Florham Park, NJ)
    …and scientific strategic and operational input into core medical affairs activities such as: healthcare professional/provider interactions (HCPs, Patients and ... activities (promotional material generation/product launches) and market access. Drives Medical Affairs input into and influences the development of asset strategy.… more
    AbbVie (08/02/24)
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  • Senior Medical Director , Medical Science…

    Mitsubishi Chemical Group (Jersey City, NJ)
    …hope for all facing illness. As a senior member of Medical Science, the Senior Director , Medical Science - Early Stage will lead the early -stage development ... therapeutic areas involving complex indications including rare disease/orphan conditions. The Senior Director , Medical Science - Early Stage will be responsible… more
    Mitsubishi Chemical Group (06/21/24)
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  • Director , Medical Science - Early

    Mitsubishi Chemical Group (Jersey City, NJ)
    …and in creating and implementing experimental medicine studies. Reporting into the Senior Director of the Medical Science Early -Stage, the Director , MSES ... 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 (06/21/24)
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  • Director , Drug Product Early

    Merck (Rahway, NJ)
    …clinical trials. Close partnership with supply chain colleagues from Quality, Regulatory Affairs , Facilities Management, Engineering, and Analytical will be ... **Job Description** The Drug Product Early Development Center in Rahway, New Jersey provides...based in New Jersey and reports to the Executive Director of FLEx Non-Sterile Operations in Pharmaceutical Operations &… more
    Merck (07/30/24)
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  • Director , Early Development Leader…

    J&J Family of Companies (New Brunswick, NJ)
    …functional area partners (eg, Translational research, Precision Medicine and diagnostics, Regulatory Affairs , Market Access, Clinical Development) to identify ... Director , Early Development Leader - Hematology,...drug development, such as translational research, clinical studies, or regulatory interactions. + Familiarity with healthcare relevant datasets, such… more
    J&J Family of Companies (07/12/24)
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  • Director , Translational Medicine (US…

    Mitsubishi Chemical Group (Jersey City, NJ)
    …2022. The company handles research, clinical development, sales, marketing, medical affairs , supply chain,and business development functions. MTPA is dedicated to ... on real-world evidence, and creating hope for all facing illness. The Director , Translational Medicine (TM), will be primarily responsible for creating plans for… more
    Mitsubishi Chemical Group (06/01/24)
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  • Global Oncology Marketing Director

    Merck (Rahway, NJ)
    …internal partners including HH, our Research & Development Division **,** Medical Affairs , Market Access, Regulatory Affairs , Legal & Compliance, ... pharma? Then you could be our new Global Marketing Director , Precision Medicine. **The position:** We are currently recruiting...to support our growing portfolio of Oncology Medicines across early stage of the diseases. The development of tumor… more
    Merck (07/31/24)
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  • Senior Director , Clinical Pharmacology

    Mitsubishi Chemical Group (Jersey City, NJ)
    …PK analysis plans, study reports, and Clinical Pharmacology sections of regulatory submissions. The Senior Director , Clinical Pharmacology also analyzes, ... 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 (06/21/24)
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  • Director Clinical Development - Respiratory

    Teva Pharmaceuticals (Parsippany, NJ)
    …as needed + Partners cross-functionally with departments such as Regulatory Affairs , Toxicology, CMC/Formulations, Biostatistics, Legal, Marketing, ... documents (ie protocols, Investigator's Brochures, clinical study reports, summaries for regulatory submissions). The Director , Clinical Development will provide… more
    Teva Pharmaceuticals (08/03/24)
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  • Senior Director , Clinical Operations

    Mitsubishi Chemical Group (Jersey City, NJ)
    …2022. The company handles research, clinical development, sales, marketing, medical affairs , supply chain,and business development functions. MTPA is dedicated to ... As a senior member of Clinical Operations, the Senior Director , Clinical Operations will lead the full development team...for the company, drawing on expertise in clinical and regulatory requirements, both local and international, related to the… more
    Mitsubishi Chemical Group (05/15/24)
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  • Senior Clinical Director , Immunology

    Merck (Rahway, NJ)
    …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... regulatory filing, and publication. **Specifically, The Senior Clinical Director May Be Responsible For:** + Evaluating pre-clinical and translational work… more
    Merck (08/01/24)
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  • Medical Director , Oncology Asset…

    Merck (Rahway, NJ)
    …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... cycle of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication. Specifically, the Director may be… more
    Merck (08/08/24)
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  • Senior Principal Scientist, Clinical Research, GYN…

    Merck (Rahway, NJ)
    …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. Specifically, the Senior Director more
    Merck (08/10/24)
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