• Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …centered around rare diseases and immune disorders. ResponsibilitiesEnsure global regulatory plans support a precision medicine approach eg integrated ... drug/diagnostic regulatory and submission plans), including HA engagement plans and...engagement plans and mitigation strategies.Ensure high quality collaboration global regulatory leads and provides guidance to the regional strategists… more
    HireLifeScience (06/22/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …or More Years in the pharmaceutical industry preferred1 or More Years in regulatory affairs requiredExperience in (s)NDA/BLA filing to FDA preferred Travel ... 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
    HireLifeScience (06/19/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, 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 (06/12/24)
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  • Eisai, Inc (Nutley, NJ)
    …If this is your profile, we want to hear from you. Summary The Associate Director is responsible for developing RWE strategies for assigned product(s) and ... #IND123 #LI-Remote Eisai Salary Transparency Language:The base salary range for the Associate Director , Global RWE (Real World Evidence), Global Medical … more
    HireLifeScience (06/25/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …for a living. Are you ready to make a difference? The Position The Associate Director , Research Partnerships (RP) is responsible for developing and executing ... alignment with the Evidence Generation Plan (EGP). Externally, the Associate Director RP will be the lead...across CDSE and more broadly within Clinical, Medical and Regulatory , Market Access and Public Affairs . Externally,… more
    HireLifeScience (06/26/24)
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  • Merck & Co. (North Wales, PA)
    …that interface with internal and external stakeholders, including US Medical Affairs , Regional Vaccine Medical Directors, Global Marketing, the Center for ... and advocacy perspective, ensuring alignment with marketing strategy Collaborate with Medical Affairs to develop and execute upon a scientific engagement plan that… more
    HireLifeScience (06/25/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …centered around rare diseases and immune disorders.Summary The Associate Director , RACMC, is responsible for the regulatory CMC (Chemistry, Manufacturing ... Regulatory guidelines and assists in educating the organization on evolving Regulatory Affairs CMC (RACMC) issues and regulations through internal technical… more
    HireLifeScience (06/07/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    … Liasions to ensure sucessful implementation of CDx and data collectionSupports Regulatory affairs in providing content and providing review of documents ... globallyCreates a forward-looking Diagnostic development strategy while keeping abreast of regulatory and policy updates in the external environment and by tracking… more
    HireLifeScience (06/18/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …as other research areas centered around rare diseases and immune disorders.SummaryThe Associate Director (AD) is responsible for overseeing all activities ... and is also an integral member of the Medical Affairs Team. This position plays a key role in...data and promotional content within the assigned therapeutic area- Regulatory milestones, actions and guidance relevant to medical review… more
    HireLifeScience (06/04/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …clinical trials is required Demonstrates technical expertise within Clinical Development, Medical Affairs , and Regulatory Affairs (CMR), staying up-to-date ... About the Department The Clinical Development, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the… more
    HireLifeScience (04/26/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …statistical results and provide input on reporting (CSR) to support Medical Affairs and HEOR/HTA strategies: Plan, set-up and execute additional statistical analyses ... Statistical deliverables. Contribute, with limited supervision, to documents submitted to Regulatory or Pricing Authorities. May participate as subject matter expert… more
    HireLifeScience (05/17/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …research areas centered around rare diseases and immune disorders. Summary The Senior Director , Head Global PV Quality (DSI/DSE) reports to the Global Head RDPVQA, ... and oversees multiple levels of direct reports (Directors, Associate Directors, Managers, contractors as applicable) across the Global PV Quality teams located in… more
    HireLifeScience (06/01/24)
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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 ... regulatory filing, and publication. Specifically, The Senior Clinical Director May Be Responsible For: Evaluating pre-clinical and translational work for… more
    HireLifeScience (05/25/24)
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  • Associate Director

    J&J Family of Companies (Cincinnati, OH)
    Associate Director , Regulatory Affairs (Instruments & Accessories) - Robotics & Digital Solutions, Inc. - 2406195848W **Description** Robotics & Digital ... of the Johnson & Johnson family of companies, is recruiting for an ** Associate Director , Regulatory Affairs ** to support our Instruments and Accessories… more
    J&J Family of Companies (06/25/24)
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  • Associate Director

    Taiho Oncology (Princeton, NJ)
    Associate Director , Regulatory Affairs Strategy Pleasanton, CA, USA * Princeton, NJ, USA Req #374 Thursday, May 30, 2024 Looking for a chance to make a ... and/or development regulatory activities under the direction of Regulatory Affairs management. The incumbent plans, directs and executes the regulatory more
    Taiho Oncology (05/31/24)
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  • Associate Director Regulatory

    Abbott (Alameda, CA)
    …to work for diversity, working mothers, female executives, and scientists. **The Opportunity** This ** Associate Director Regulatory Affairs - APAC** will ... CA, location in the Diabetes Division. As a manager, the function of an Associate Director Regulatory Affairs , APAC (Asia Pacific) is to combine… more
    Abbott (06/06/24)
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  • Associate Director

    BD (Becton, Dickinson and Company) (Covington, GA)
    **Job Description Summary** As Associate Director , Regulatory Affairs , you will be responsible for managing a team that develops and executes the ... updates, risks and regulation or guidance changes to Corporate Quality and Regulatory Affairs . International Regulatory Affairs and Senior Leadership.… more
    BD (Becton, Dickinson and Company) (04/09/24)
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  • Associate Director

    Novo Nordisk (Princeton, 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 (05/09/24)
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  • Associate Director

    Abbott (Sylmar, CA)
    …work for diversity, working mothers, female executives, and scientists. **The Opportunity** This ** Associate Director , Regulatory Affairs ,** will work in ... helpful. + Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society.) + Previous experience with 510k and CLIA waiver submissions.… more
    Abbott (06/21/24)
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  • Associate Director

    Regeneron Pharmaceuticals (Tarrytown, NY)
    The Associate Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will ... mainly focus on Clinical Regulatory filings and provide regulatory leadership on the project teams in this area. We are a hands-on culture so responsibilities… more
    Regeneron Pharmaceuticals (05/11/24)
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