• Senior Administrative Lead, Coding

    LogixHealth (Bedford, MA)
    …education E/M manual + Creation of coder quality reports /tableau dashboards + Ac tasS har ePointAdminist ra torforCo di ngPo li c ie s , Co der Au di ts , Education ... l ity: + Ab ili tytoa dd, tos ubt ra ct , mult iply and di v ide...uc hassa fe tyru le s , o pe ra tingandmainte nan ceinstr uct ions and proc ed...tingandmainte nan ceinstr uct ions and proc ed u ra lm an uals + Ab ili tyto wr… more
    LogixHealth (08/04/25)
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  • Director, Global Regulatory Sciences

    Pfizer (Cambridge, MA)
    …Requirements)** + BS is required. MS, PharmD, or PhD preferred + Prior clinical regulatory affairs experience in vaccines is required, at least 8 years. + ... to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned. Regulatory Affairs more
    Pfizer (08/22/25)
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  • Principal Reg Affairs Specialist

    Medtronic (Boston, MA)
    …in a more connected, compassionate world. **A Day in the Life** Job Summary: Principal Regulatory Affairs Specialist As a Principal Regulatory Affairs ... Specialist, you will play a key role in ensuring regulatory compliance and supporting the global market expansion of products commercialized by Digital Technologies.… more
    Medtronic (08/21/25)
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  • Senior Principal Scientist, Translational…

    Merck (Boston, MA)
    …scientists (including discovery research, biostatistics, drug metabolism, modeling and simulation, regulatory affairs , and global clinical trials operations) + ... Translational Medicine Operations, Translational Medicine-EU, Drug Metabolism/Modeling & Simulation, Regulatory Affairs , and late-stage Clinical Research throughout… more
    Merck (08/16/25)
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  • VP Clinical Development, Oncology

    Sumitomo Pharma (Boston, MA)
    …budget for Oncology clinical development activities. + Partner with Translational Research, Regulatory Affairs , Clinical Operations, and Medical Affairs to ... submissions, clinical study reports, and NDA/MAA filings. + Collaborate with regulatory affairs team to ensure compliance with regulatory requirements. **Key… more
    Sumitomo Pharma (08/14/25)
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  • R&D Regulatory Manager

    Grifols Shared Services North America, Inc (Worcester, MA)
    …8 or more years of experience in positions of increasing responsibility within Regulatory Affairs or related field within the Biologics, Biotech or ... Hiring Ordinance.** Learn more about Grifols (https://www.grifols.com/en/what-we-do) **Req ID:** 527460 **Type:** Regular Full-Time **Job Category:** Regulatory Affairs more
    Grifols Shared Services North America, Inc (08/01/25)
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  • Head of Product Quality & Lifecycle Management,…

    Takeda Pharmaceuticals (Lexington, MA)
    …liaison between Biologics Business Unit senior management and Global Quality, Regulatory Affairs , and Operations, fostering seamless communication and decisive ... and processes + Broad knowledge and experience within the GMP environment, and regulatory affairs + Thorough understanding of applicable regulations and guidance… more
    Takeda Pharmaceuticals (07/30/25)
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  • Clinical Lead, Early Clinical and Experimental…

    Sanofi Group (Cambridge, MA)
    …Clinical Operations (EDCO, including Clinical Trial Managers and Data Managers), Regulatory Affairs , Patients Safety & Pharmacovigilance, Therapeutic Area ... Clinical Operations (EDCO, including Clinical Trial Managers and Data Managers), Regulatory Affairs , Patients Safety & Pharmacovigilance, Therapeutic Area… more
    Sanofi Group (07/29/25)
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  • Sr. Director, Global Market Access and Pricing…

    Sanofi Group (Cambridge, MA)
    … etc.) + Partner effectively with relevant departments (eg Commercial, Clinical Development, Regulatory Affairs , Medical Affairs , HEOR ) to influence the ... Regular, close contact with: + GPT members (NPP/GBL, GPH, GPM, Clinical leads, Regulatory Affairs leads, Medical ) + HEVA leads + Major Local Market Access… more
    Sanofi Group (07/23/25)
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  • Medical Director, Global Medical Affairs

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …value and real-world evidence, US and global commercial teams, market access, and regulatory affairs , to ensure integrated global strategies and cohesive medical ... (T0 - T1) or early development (phase 1) assets either within Medical Affairs , Regulatory Affairs , or Clinical Development is preferred. + Minimum of 7+… more
    Otsuka America Pharmaceutical Inc. (07/16/25)
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