• Director , Global Regulatory

    Takeda Pharmaceuticals (Lexington, MA)
    …and approves - as needed - technical protocols, reports, etc. to ensure alignment with global regulatory requirements and standards. + When in a GRA CMC Product ... life-changing therapies to patients worldwide. Join Takeda as a Director GRA CMC where you will independently develop and...regulatory guidance to product teams in line with global regulatory strategies. Accountable for development and… more
    Takeda Pharmaceuticals (11/10/24)
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  • Director , Global Regulatory

    AbbVie (Waltham, MA)
    …Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Director Regulatory Affairs Global Regulatory ... approval for product(s) in the assigned therapeutic area. Leads the Global Regulatory Product Team (GRPT). Continually expands TA knowledge, and ensures… more
    AbbVie (09/20/24)
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  • Medical Director , Medical Affairs

    AbbVie (Waltham, MA)
    …assist with the scientific review, development, execution and communication of affiliate/area/ global medical affairs sponsored or supported clinical research ... preferred. Will consider remote candidates. Purpose: The Associate Medical Director /Associate Scientific Director provides specialist medical/scientific strategic… more
    AbbVie (10/18/24)
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  • Associate Director , US Advertising…

    Takeda Pharmaceuticals (Lexington, MA)
    …of proposed promotional and disease state materials. + Collaborate with Regulatory Affairs , Medical, Legal, Commercial, and Compliance, execute and ... and compliance with regulatory requirements. + Understand broad concepts within Regulatory Affairs and potential effects across the organization. Identify … more
    Takeda Pharmaceuticals (11/15/24)
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  • Global Medical Director , Allergy

    ThermoFisher Scientific (Waltham, MA)
    …highly motivated and experienced individual to join our team as Global Medical Director , Allergy on the Medical and Scientific Affairs (MSA) team. In this ... quality and innovation. As part of a successful, growing global organization you will be encouraged to perform at...different departments, such as marketing, sales, manufacturing, quality and regulatory affairs . You will also collaborate with… more
    ThermoFisher Scientific (09/27/24)
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  • Director , Global Health Economics…

    Olympus Corporation of the Americas (Westborough, MA)
    …an entity other than @Olympus.com, it is likely not legitimate._ **Job Description** The Director , Global Health Economics & Market Access is part of Health ... Market Access (HEMA) function and reports directly to Executive Director , Global Health Economics & Market Access....and policy makers + Coordinate with Medical & Clinical Affairs , Regulatory to ensure appropriate support and… more
    Olympus Corporation of the Americas (08/23/24)
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  • Global Benefits Director Job Details…

    Black & Veatch (Burlington, MA)
    ** Global Benefits Director ** Date: Oct 22, 2024 Location: Overland Park, KS, US US Company: Black & Veatch Family of Companies **Together, we own our company, ... questions and put your diverse talents and perspectives to use. **The Opportunity** The ** Global Benefits Director ** will have the opportunity to: + Lead the… more
    Black & Veatch (10/24/24)
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  • International Medical Director

    Novo Nordisk (Lexington, MA)
    …Clinical Operations, Non-Clinical Research, Medical Writing, Program Management, CMC and Regulatory Affairs teams. Will be interfacing with both internal ... About the Department Our East Coast Global Development Hub brings together the best minds...Operations, Non-Clinical Research, Medical Writing, Program Management, CMC and Regulatory Affairs teams to deliver and drive… more
    Novo Nordisk (10/17/24)
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  • Senior Manager, US Medical Ad/Promo…

    Takeda Pharmaceuticals (Lexington, MA)
    …potential issues. **POSITION ACCOUNTABILITIES:** + Collaborate with colleagues in Regulatory Affairs , Medical, Legal, Commercial, and Compliance organizations ... the US Medical team, you will report to the Director , Ad/Promo Regulatory Review. You will be... regulatory requirements. + Understand broad concepts within Regulatory Affairs and potential effects across the… more
    Takeda Pharmaceuticals (11/15/24)
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  • Director , Business Development Quality…

    Olympus Corporation of the Americas (Westborough, MA)
    …adequate support at global and regional levels. + Ensure the appropriate global regulatory requirements, are considered as part of due diligence and ... is maintained, well-organized and ready to be audited by global regulatory authorities / notified bodies. +...preferred. + Minimum of 15 year of directly related Regulatory Affairs experience; preferably a minimum of… more
    Olympus Corporation of the Americas (10/24/24)
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  • Associate Director , US Medical…

    Takeda Pharmaceuticals (Lexington, MA)
    …Field Medical, Medical Information, Program Management; other USBU Stakeholders; and Global functional groups such as Medical, Publications, Regulatory , ... Description** About the role Join Takeda as an Associate Director , US Medical Communications - Gastroenterology where you will...new products + In collaboration with the US Medical Affairs team, support development and execution of the Medical… more
    Takeda Pharmaceuticals (11/15/24)
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  • Associate Director , US 3PL Operations…

    Takeda Pharmaceuticals (Lexington, MA)
    …and resolution + Set and maintain all relevant SOPs with Operations, Tax, Regulatory Affairs and Quality + Sustain GDP compliance and support Internal/External ... the best of my knowledge. **Job Description** **Job Title** : Associate Director , US 3PL Operations Management Lead (Operations & Analytics) **Location** :… more
    Takeda Pharmaceuticals (11/13/24)
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  • User Experience and User Interface Designer

    Takeda Pharmaceuticals (Lexington, MA)
    …+ Collaborate cross-functionally with engineering, human factors, quality, clinical & medical affairs , regulatory affairs , commercial, legal, and purchasing. ... graphic design demanding a deep understanding of user behaviors, regulatory requirements, and the intricate nuances of medical device...of the Product Design team, you will report to Director , Product Design. **How you will contribute:** + Develop… more
    Takeda Pharmaceuticals (08/23/24)
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  • Senior Clinical Pharmacology Specialist

    Novo Nordisk (Lexington, MA)
    …writing, Regulatory , Data Science (statistics, pharmacometrics), Research and Early Development, Global Translation, Global Medical Affairs , Global ... About the Department Our East Coast Global Development Hub brings together the best minds...may involve some travel. Relationships Reports to the Senior Director , Clinical Pharmacology for the US East Coast Hub.… more
    Novo Nordisk (09/13/24)
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