• Director Regulatory Affairs Liaison-…

    Merck (Boston, MA)
    **Job Description** Our Regulatory Affairs team bring new medical advancements to the world by facilitating communications and procedures that allow swift, ... **Looking for someone with a growth mindset. The Director, Regulatory Affairs Liaison is responsible for:** +...not limited to:** + Reports to Executive Director or Associate Vice President, Therapeutic Area Lead. + Develops worldwide… more
    Merck (05/22/24)
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  • Student Nurse Technician

    Veterans Affairs, Veterans Health Administration (Bedford, MA)
    …Internship opportunities within the Department of Veterans Affairs , please visit: https://www.va.gov/EMPLOYEE/pathways-internship-program/. Incumbent will be given ... program is a requirement for all Department of Veterans Affairs Health Care Personnel (HCP) Participation in the Coronavirus...of 2 academic years of post-high school study or associate 's degree in the field of nursing. The required… more
    Veterans Affairs, Veterans Health Administration (03/26/24)
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  • Associate Director, Global…

    Takeda Pharmaceuticals (Boston, MA)
    Regulatory Affairs Team. **How you will contribute:** + As Associate Director, Global Regulatory Project Management and Strategic Planning, you will ... process changes through proactive engagements with cross functional team members, Global Regulatory Affairs TAU colleagues and Global Regulatory Project… more
    Takeda Pharmaceuticals (06/07/24)
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  • Senior Manager, Global Regulatory Labeling…

    Takeda Pharmaceuticals (Boston, MA)
    …in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director, Global Labeling Lead where you will be responsible for the ... negotiations with Health Authorities. + Ensures labeling content conform to regulatory requirements. Management of Local Exceptions and LOC Interactions + Manages… more
    Takeda Pharmaceuticals (06/18/24)
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  • Associate Director, Global Labeling

    Takeda Pharmaceuticals (Boston, MA)
    …You will serve as the regulatory expert for labeling on the Global Regulatory Affairs subteam to ensure that regulatory labeling requirements are met ... life-changing therapies to patients worldwide. Join Takeda as an Associate Director, Global Labeling Lead where you will be...+ Acceptable and independent skills in the area of regulatory affairs such as understanding broad concepts… more
    Takeda Pharmaceuticals (06/07/24)
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  • Pricing and Contracts Specialist (USA…

    Danaher Corporation (Boston, MA)
    …a dynamic team of cross-functional stakeholders including sales, service, finance, legal, regulatory affairs , etc. The essential requirements of the job include: ... Department located in Coralville, Iowa and will be fully remote . At IDT, we are one global team....+ Bachelor's degree in business or related field OR Associate 's degree with 2 years IDT experience + Excellent… more
    Danaher Corporation (06/19/24)
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  • Associate Director, Global Labeling Lead

    Takeda Pharmaceuticals (Boston, MA)
    …in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director, Global Labeling Lead where you will be responsible for the ... and assures that Takeda labeling content and processes conform to regulatory requirements. Management of Local Exceptions and LOC Interactions + Manages… more
    Takeda Pharmaceuticals (06/13/24)
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  • Associate General Counsel

    Children's Hospital Boston (Boston, MA)
    75978BRJob Posting Title: Associate General CounselDepartment:General CounselAutoReqId:75978BRStatus:Full-TimeStandard Hours per Week:40 Job Posting Category:Legal, ... role will serve as the primary point of contact for legal affairs at Franciscan Children's and other affiliated organizations, providing strategic legal guidance… more
    Children's Hospital Boston (06/21/24)
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  • Senior Clinical Director, Immunology

    Merck (Boston, MA)
    …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. **Specifically, The Senior Clinical Director May… more
    Merck (05/25/24)
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