• Associate Director, Regulatory Operations

    Rhythm Pharmaceuticals (Boston, MA)
    …life/physical sciences or related field + 8+ years of highly relevant pharmaceutical /biotechnology experience in Regulatory Affairs Operations + Knowledge and ... understanding of the drug development process + Strong knowledge of FDA and Global EU/UK regulations and guidelines, especially CTD and eCTD structure + Experience with Veeva RIM EDMS + Highly proficient in Microsoft Office suite + Ability to balance both… more
    Rhythm Pharmaceuticals (07/30/25)
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  • Medical Science Liason

    Astrix Technology (Boston, MA)
    …discipline. + Experience: Minimum of 2 years in a field-based medical affairs role within the pharmaceutical , biotechnology, or medical device industry. ... join us! Our partners range from emerging biotech firms to established pharmaceutical companies, all seeking professionals who can bridge scientific insights with… more
    Astrix Technology (08/11/25)
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  • Director, Quantitative Clinical Pharmacology Lead

    Takeda Pharmaceuticals (Cambridge, MA)
    …Pharmacometrics, Statistics, Drug Safety, Clinical Sciences, Outcomes, Digital Health, Pharmaceutical Sciences/Device, and Global Regulatory Affairs . + Advanced ... drive a MIDD path within each At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To… more
    Takeda Pharmaceuticals (06/27/25)
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  • Senior/Patient Advocacy & Medical Society…

    United Therapeutics (Boston, MA)
    …are as follows:** Who We Are We are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit corporation. Our public benefit ... a brighter future for patients through the development of novel pharmaceutical therapies; and technologies that expand the availability of transplantable organs.… more
    United Therapeutics (08/23/25)
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  • Team Lead - Scale Up Lab Support

    ThermoFisher Scientific (Cambridge, MA)
    …(SUBs), wave reactors preferred. Demonstrated knowledge of cGMPs/GLP or regulatory affairs pertaining to the pharmaceutical and biological industries is ... preferred. Knowledge of gene therapy product and/or process development preferred. Excellent problem solving and critical thinking skills, including strong attention to detail. Advise supervisor of factors that may affect quality, accuracy, timeliness, and… more
    ThermoFisher Scientific (06/20/25)
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  • Senior Manager, US Medical Information and Review

    Takeda Pharmaceuticals (Lexington, MA)
    …information / clinical expertise for assigned products to internal (Medical Affairs strategy teams, Therapeutic Area Units within R&D, commercial Brand teams) ... 2) medical and scientific slides housed in the Medical Affairs slide repository, and 3) other relevant publications in...MD or Ph.D., with a thorough grasp of the pharmaceutical industry. * 2-3 years of healthcare or related… more
    Takeda Pharmaceuticals (08/15/25)
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  • Sr Dir Pharmacy Trade Relations - Remote

    Prime Therapeutics (Boston, MA)
    …Pharmacy Trade Relations - Remote **Job Description** The Sr Director, Pharmaceutical Trade Relations is responsible for managing Prime's Trade Relations program(s) ... and market access strategies and all related partner/customer relationships including pharmaceutical manufacturers, with specific emphasis on Medicare Part D and… more
    Prime Therapeutics (08/08/25)
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  • Associate Director, Clinical Research, Value…

    Takeda Pharmaceuticals (Lexington, MA)
    …execution of all US Medical Clinical Research including, Medical Affairs Company Sponsored Studies (MACS) collaborative studies and Investigator Initiated ... AND ASPECTS_** **Technical/Functional Expertise** + Comprehensive understanding of the pharmaceutical industry and regulations governing medical functions within industry… more
    Takeda Pharmaceuticals (08/02/25)
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  • Senior Principal Scientist, Translational…

    Merck (Boston, MA)
    …seeking a highly qualified physician-scientist with a proven track record in the pharmaceutical industry as well as independent academic research for a position in ... The preferred candidate will have at least 5-year experience in the pharmaceutical industry and Immunology R&D and clinical and academic expertise in… more
    Merck (08/16/25)
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  • Associate Director, Product Quality

    AbbVie (Waltham, MA)
    …agency regulations worldwide. Products include regulatory starting materials, Active Pharmaceutical Ingredients (API), Intermediates, and Drug Products produced by ... Commercial, Global Supply Chain, Domestic and International AbbVie Plants and Affiliates, Regulatory Affairs , R&D, and S&T to ensure alignment on strategic in + Lead… more
    AbbVie (07/11/25)
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