• Merck & Co. (North Wales, PA)
    …with Global Medical and Scientific Affairs (GMSA), US, Senior Director of Medical Affairs (SDMA), Center for Observational and Real-world Evidence (CORE), ... Job DescriptionJob Description:The Associate Director , Marketing, HPV Scientific Strategy plays a critical...Policy, Vaccine Scientific Engagement (VSE), and Global Marketing to lead scientific commercial activities… more
    HireLifeScience (11/09/24)
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  • Merck & Co. (North Wales, PA)
    Job DescriptionThe US Director of Precision Medicine will lead the national lab strategy, diagnostic collaboration, and partnerships across the US market. This ... teamsIn addition, lead the non-oncology therapeutic areas in coordination with Global Precision Medicine for brand support from a US market diagnostic and… more
    HireLifeScience (11/09/24)
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  • Merck & Co. (North Wales, PA)
    Job DescriptionUnder the guidance of a senior leader , the Principal Scientist, Outcomes Research-Women's Cancer has primary responsibility for developing value ... development of American Managed Care Pharmacy (AMCP) dossiers for US payers, and Global Value Dossiers for use by local subsidiaries in their HTA submissions. The… more
    HireLifeScience (11/08/24)
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  • Merck & Co. (North Wales, PA)
    Job DescriptionOur company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we ... an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated… more
    HireLifeScience (11/09/24)
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  • Associate Director , Global

    Takeda Pharmaceuticals (Trenton, NJ)
    …our Global Regulatory Affairs organization, based remotely. + Partners with the Global Regulatory Lead (GRL) on Global Regulatory Teams ... empower you to shine? Join us as an Associate Director , Global Regulatory Project Management...**How you will contribute:** + Partnering with the program Global Regulatory Lead (GRL), co-… more
    Takeda Pharmaceuticals (10/24/24)
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  • Director , Global Regulatory

    J&J Family of Companies (Titusville, NJ)
    Director , Global Regulatory Leader (GRL) - 2406184564W **Description** Johnson & Johnson Innovative Medicine is recruiting for a Director , Global ... more at www.janssen.com . Key Responsibilities: + Bring innovative regulatory approaches, deeply rooted in science, to lead...exist + Integrate multiple inputs from regional and functional Global Regulatory Team members to build coherent… more
    J&J Family of Companies (09/06/24)
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  • Director , Global Regulatory

    Merck (Upper Gwynedd, PA)
    …and obtain shortest time to approval by regulatory agencies. + Functions as global regulatory lead assigned to programs where the compound is ... **Job Description** We are seeking a Director (Principal Scientist), Global Regulatory...submissions and associated documentation. + Provides expertise as the Global Regulatory Lead to Product… more
    Merck (10/31/24)
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  • Senior Principal Scientist (Senior Director

    Merck (North Wales, PA)
    …review and final approval for all submissions and associated documentation. Provides expertise as Global Regulatory Lead to Product Development Teams and ... seeking a Senior Director (Sr. Principal Scientist) Global Regulatory Affairs Liaison with a visionary,...targeted product labeling + Provide expert advice as the Global Regulatory Lead to Product… more
    Merck (10/31/24)
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  • Associate Director - CMC Regulatory

    Lilly (Philadelphia, PA)
    …people around the world. **Position Overview:** The Associate Director - CMC Regulatory is responsible for leading global CMC regulatory activities for ... better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana....for the generation and execution of country specific CMC regulatory strategies + Lead CMC regulatory more
    Lilly (08/24/24)
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  • Associate Director , Global Labeling…

    Takeda Pharmaceuticals (Trenton, NJ)
    …Management + Appropriately escalates issues to Global Labeling management and the Global Regulatory Lead (GRL) and proposes risk mitigation strategies ... life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where...+ Working within Labeling Team and GRA + Represents Global Labeling at Global Regulatory more
    Takeda Pharmaceuticals (10/16/24)
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  • Senior Director , Global Labeling…

    Bristol Myers Squibb (Princeton, NJ)
    …to:** + New Product Portfolio working closely with their TA counterparts in Global Regulatory Strategy, Worldwide Patient Safety (WWPS), Clinical Development and ... and maintenance of global compliant labels. Position will also serve as Global Labeling Lead for assigned products. **Responsibilities include, but are not… more
    Bristol Myers Squibb (11/10/24)
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  • Associate Director , CMC Regulatory

    J&J Family of Companies (Horsham, PA)
    … strategy through partnership and communication with Therapeutic Area Regulatory Affairs ( Global Regulatory Leader ). + Refines regulatory strategies ... Associate Director , CMC Regulatory Affairs - 2406221330W...**Key Responsibilities:** + Provides guidance and expertise to the Global Regulatory Team to develop global more
    J&J Family of Companies (11/07/24)
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  • Director , Regulatory Medical…

    J&J Family of Companies (Spring House, PA)
    Director , Regulatory Medical Writing (1 of 4) - 2406211847W **Description** Johnson & Johnson is currently seeking a Director , Regulatory Medical ... potential. At Johnson & Johnson, we all belong. The Director , Regulatory Medical Writing (RegMW) is a...plan, assessment aid) documents is preferred. + Knowledge of global regulations, regulatory timelines, guidelines, and … more
    J&J Family of Companies (11/07/24)
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  • Associate Director , Nonclinical…

    Takeda Pharmaceuticals (Trenton, NJ)
    …cross-functional team members (Clinical, Global Patient Safety, Program Management, Global Regulatory , Regulatory Operations, Drug Discovery Units, ... the best of my knowledge. **Job Description** **About the role:** **Associate Director , Nonclinical Regulatory Writing and Submission Support,** **_Oncology and… more
    Takeda Pharmaceuticals (09/19/24)
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  • Executive Director , Device Quality…

    Merck (Trenton, NJ)
    … CMC Oversight + Lead the preparation and submission of high-quality regulatory CMC device content for global submissions, including IND, NDA, BLA, and ... **Job Description** The Executive Director , Device Quality & Regulatory will... regulatory guidelines and trends. + Collaborate with global regulatory teams to align strategies and… more
    Merck (11/09/24)
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  • Director , Translational Medicine and Early…

    Organon & Co. (Plymouth Meeting, PA)
    …**The** **Position** **This position can be 100% remote in the US** The Director , Translational Medicine and Early Development (TMED) Lead will be responsible ... are sound, based on the most up-to-date literature and regulatory guidances and support the approved early development plans....for the execution (in conjunction with the TMED Operations Lead ) and reporting thereof. The Director will… more
    Organon & Co. (10/17/24)
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  • Director Global Oncology Marketing…

    Merck (North Wales, PA)
    Global Oncology Marketing** for Lung cancer for our Company's oncology business. The Global Marketing Director will lead strategies and marketing efforts ... in Rahway, NJ and will report to the Executive Director , Global Marketing for NSCLC. The position...NSCLC working in conjunction with Precision Marketing team + Lead in liaising with Outcomes Research, Global more
    Merck (11/02/24)
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  • Director , Biologics VCM Product…

    Merck (West Point, PA)
    …Continuity Planning (BCP), including identification & prioritization of mitigation strategies + Lead Global Filing and Launch (GFLS) strategy development to gain ... Leader will be responsible for supply chain design, global filing and launch strategy, long-range demand vs capacity...continuity of supply, and commercial outcomes. The VCM Product Leader will lead the cross-functional Supply Chain… more
    Merck (11/06/24)
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  • Associate Director , Global Patient…

    Takeda Pharmaceuticals (Trenton, NJ)
    …of clinical trial and Pharmacovigilance methodologies including detailed comprehension of global regulatory requirements. + Good cross-cultural understanding and ... therapies to patients worldwide. Join Takeda as an Associate Director , Global Patient Safety Clinical Operations in...Clinical Development Program issues/risks in a proactive matter and lead discussions to mitigate them + Perform tasks of… more
    Takeda Pharmaceuticals (11/10/24)
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  • Clinical Development Lead

    Bristol Myers Squibb (Princeton, NJ)
    …to meet regulatory , quality, medical, and access goals + Serves as a matrix leader to lead , develop, motivate and achieve results through teams, and is the ... . **Position Summary** + CDLs are matrix leaders and managers who lead , develop, motivate and achieve results through teams; demonstrate a commitment to… more
    Bristol Myers Squibb (11/10/24)
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