We interpreted Morrisville, PA as Morrisville, PA. Other options include: Morrisville (Greene County), PA

  • Novo Nordisk Inc. (Plainsboro, NJ)
    …you ready to make a difference? The Position We are seeking a collaborative and science -driven global regulatory expert who wants to work with innovative ... Development Hub brings together the best minds in life science innovation with facilities in Lexington, MA and Plainsboro,...functional areas. Relationships You will report to the Senior Director - Global Regulatory Portfolio… more
    HireLifeScience (01/18/25)
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  • Genmab (Plainsboro, NJ)
    …and authentic is essential to fulfilling our purpose.The RoleThe Global Regulatory Labeling Strategy Sr Manager/Associate Director will be responsible for ... to our business, which is innovative and rooted in science , we believe that being proudly unique, determined to...Genmab portfolio of products. This role will be within Global Regulatory Affairs (GRA) and will report… more
    HireLifeScience (11/15/24)
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  • Genmab (Plainsboro, NJ)
    …authentic is essential to fulfilling our purpose.The RoleGenmab is searching for an experienced Director , Global Clinical Drug Supply to be part of Global ... to our business, which is innovative and rooted in science , we believe that being proudly unique, determined to...bringing medicines to cancer patients and other serious diseases. Director , Global Clinical Drug Supply will work… more
    HireLifeScience (01/07/25)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …Affairs (MAPA), as well as collaborating where appropriate with therapeutically aligned global counterparts in Medical Science , Patient Focused Drug Development, ... Data Science and Global Evidence and Pricing Access. In addition, the Director will represent Novo Nordisk externally and assume a leadership role in… more
    HireLifeScience (01/22/25)
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  • Genmab (Plainsboro, NJ)
    …caring, candid, and impact-driven to our business, which is innovative and rooted in science , we believe that being proudly unique, determined to be our best, and ... authentic is essential to fulfilling our purpose.The RoleThe Global Clinical Trial Manager (GCTM) is accountable for the end-to-end delivery of a single or multiple… more
    HireLifeScience (12/04/24)
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  • Genmab (Plainsboro, NJ)
    …caring, candid, and impact-driven to our business, which is innovative and rooted in science , we believe that being proudly unique, determined to be our best, and ... and growing organization? At Genmab, we're seeking a Senior Director , Strategic Planning & Effectiveness to drive cross-functional communication, alignment… more
    HireLifeScience (01/17/25)
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  • Genmab (Plainsboro, NJ)
    …caring, candid, and impact-driven to our business, which is innovative and rooted in science , we believe that being proudly unique, determined to be our best, and ... authentic is essential to fulfilling our purpose.Job Description - Director , Digital Assets, Information SecurityPosition Summary: The Director Information… more
    HireLifeScience (12/04/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …make a difference? The Position Reporting to the head of Clinical, medical, Regulatory (CMR) Business Operations, the Associate Director (AD) is responsible for ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one...stakeholders. In the execution of specific projects, the Associate Director , will be accountable for managing relationships with internal… more
    HireLifeScience (01/11/25)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …Nordisk, you will have the opportunity to build a life-changing career in a global business environment. We encourage our employees to make the most of their talent, ... Are you ready to maximize your potential with us? The Position The Associate Director , Data & Analytics Governance is responsible for the governance of NNI data… more
    HireLifeScience (01/07/25)
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  • Genmab (Plainsboro, NJ)
    …needs of the US healthcare market through collaboration with US Commercialization, Global Medical Affairs, Clinical Development, Regulatory , and other cross ... to our business, which is innovative and rooted in science , we believe that being proudly unique, determined to...authentic is essential to fulfilling our purpose.The Role The Director of US Medical Affairs Solid Tumors Strategy will… more
    HireLifeScience (12/11/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …lives for a living. Are you ready to make a difference? The Position The Director , Clinical Informatics in the Clinical Data Science & Evidence (CDSE) department ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one...with other CDSE functions, CMR functions, broader NNI and Global functions to ensure local market needs are met.… more
    HireLifeScience (11/28/24)
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  • Novo Nordisk Inc. (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 collecting… more
    HireLifeScience (11/28/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …from Medical Affairs, Clinical Data Science & Evidence, legal, regulatory affairs, global publication team, and commercial publications colleagues from ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one...Manager - Publications works with minimal direction from a Director Level Team Member on the efficient and compliant… more
    HireLifeScience (01/17/25)
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  • Associate Director , Global

    Takeda Pharmaceuticals (Trenton, NJ)
    …that will inspire you and empower you to shine? Join us as an Associate Director , Global Regulatory Project Management and Strategic Planning - GI2 TAU ... within our Global Regulatory Affairs organization, based remotely. +...behaviors. **Minimum Requirements/Qualifications:** + Bachelors degree required. Emphasis in Science preferred. Advanced degree preferred + Ideal candidate has… more
    Takeda Pharmaceuticals (01/22/25)
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  • Director , Quantitative Sciences

    Merck (West Point, PA)
    …coaching/guidance to individual contributors + Maintaining a comprehensive understanding of global regulatory expectations for small molecules and biologics, ... **Job Description** **R5 -** ** Director - Pharmacometrics,** **Quantitative Pharmacology and Pharmacometrics** _T_ _he (remote) position is only applicable for those… more
    Merck (11/26/24)
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  • Medical Director , Endocrine Medical…

    Ascendis Pharma (Princeton, NJ)
    …Medical Sciences team for the US business, the Medical Director handles deliverables and activities associated with management and implementation of phase ... Medical Director Do you want to be part of...Regulatory , Clinical Development, Clinical Operations, Compliance, Pharmacovigilance, Biometrics, Global Communications, and other functional group contributors to ensure… more
    Ascendis Pharma (12/10/24)
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  • Associate Director , Regulatory

    Taiho Oncology (Princeton, NJ)
    …of regulatory affairs management, the incumbent independently prepares and directs global regulatory affairs activities and provides regulatory guidance ... Associate Director , Regulatory Affairs Strategy Princeton, NJ,...Performance Objectives: + Independently directs as well as prepares global regulatory affairs strategies and executes … more
    Taiho Oncology (11/28/24)
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  • Principal Scientist/ Director

    Merck (Trenton, NJ)
    …Combinations CMC (Chemistry, Manufacturing & Controls), you will report to the Director of Device Regulatory Affairs for Autoinjector Development Programs. You ... will spearhead regulatory activities for Devices and Drug-Device Combinations (DDDC), ensuring...a collaborative environment + Maintain in depth knowledge of global device and drug/biologic-device combination product guidelines and policy… more
    Merck (01/14/25)
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  • Associate Director , Regulatory

    Bristol Myers Squibb (Princeton, NJ)
    …more: careers.bms.com/working-with-us . **Position Responsibilities** + Leadership responsibility for global regulatory strategy to support the development of ... + Ensure global development plans will meet global regulatory requirements by soliciting and integrating...single vision as inspiring as Transforming patients' lives through science (TM) , every BMS employee plays an integral… more
    Bristol Myers Squibb (01/22/25)
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  • Associate Director , Regulatory

    Merck (West Point, PA)
    …Discovery, Preclinical and Translational Medicine Operations (DPTM) is seeking an Associate Director to lead the Molecular lab within the Late Development (AdVAnce) ... we will combine the power of innovative robotics, IT platforms, and science to accelerate vaccines and enable late-stage clinical trials through the generation… more
    Merck (12/12/24)
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