• Senior Specialist, Medical Writing

    Edwards Lifesciences (Boston, MA)
    …and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating ... in a related field with 5 years of related experience working in medical affairs , clinical affairs and/or clinical science **What else we look for (preferred):**… more
    Edwards Lifesciences (09/27/25)
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  • Director, Quantitative Clinical Pharmacology Lead

    Takeda Pharmaceuticals (Cambridge, MA)
    …lead to drive a MIDD path within each project. + Leads strategic, scientific , and operational aspects of multiple drug development projects with a high level ... and Quantitative Sciences (DQS) to the R&D organization and the external scientific community through high-value participation at scientific meetings and… more
    Takeda Pharmaceuticals (09/25/25)
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  • Senior Director, Global Regulatory Lead - Oncology

    Takeda Pharmaceuticals (Boston, MA)
    …in or lead regulatory and company initiatives. Based on experience and scientific strengths, expands knowledge of TA and provides coaching and mentoring for ... resource gaps for assigned project(s). **Minimum Requirements/Qualifications:** + BSc/BA Degree, scientific discipline strongly preferred. + Advanced degree in a … more
    Takeda Pharmaceuticals (11/01/25)
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  • Global Medical Director - Hemophilia

    Sanofi Group (Cambridge, MA)
    …+ Accountable for implementing stakeholder engagement, medical education, and scientific communication plans aligned with the strategic priorities of the ... and cross-functional teams. + Deploy innovative tools and channels for scientific communication and data dissemination, such as omnichannel and AI-based approaches.… more
    Sanofi Group (09/12/25)
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  • Associate Director, Global Regulatory Project…

    Takeda Pharmaceuticals (Boston, MA)
    …Management and Strategic Planning - Oncology TAU within our Global Regulatory Affairs organization, based remotely. + Partners with the Global Regulatory Lead (GRL) ... through proactive engagements with cross functional team members, Global Regulatory Affairs TAU colleagues and Global Regulatory Project Management and Strategic… more
    Takeda Pharmaceuticals (11/21/25)
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  • Principal Scientist, Clinical Research, Immunology

    Merck (Boston, MA)
    …closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development projects + ... company and competitors' drugs and internal and external expert opinion on scientific questions relevant to his/her areas of responsibility. **The Clinical Director… more
    Merck (11/22/25)
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  • Head of Clinical Excellence & Innovation

    Pfizer (Cambridge, MA)
    …adoption of innovative trial designs while upholding the highest standards of scientific rigor and regulatory excellence. + **Team Leadership & Culture:** Inspire, ... + **External Engagement:** Act as a visible ambassador for Pfizer at scientific conferences, regulatory forums, and partner or investor engagements - articulating… more
    Pfizer (11/23/25)
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  • Vaccine Customer Representative - Western South…

    Merck (Boston, MA)
    …field-based employees such as the Vaccine Key Customer Leader (VKCL), Vaccine Medical Affairs Leader (VMAL), Region Medical Director (RMD) as well as other members ... and health care environment knowledge through self-study of company-provided scientific , product and marketplace information, attendance at product workshops and… more
    Merck (11/05/25)
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  • Clinical Lead, Early Clinical and Experimental…

    Sanofi Group (Cambridge, MA)
    …a positive, collaborative mindset. + Take an active part in the scientific challenges involved in early clinical development, which require a scientifically ... (EDCO, including Clinical Trial Managers and Data Managers), Regulatory Affairs , Patients Safety & Pharmacovigilance, Therapeutic Area Research & Development… more
    Sanofi Group (10/07/25)
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  • GRA Device Associate

    Sanofi Group (Cambridge, MA)
    …could be critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team is a globally diverse team supporting the medical device, ... creates and maintains strong collaborative working relationships with Global Regulatory Affairs (GRA), Regional GRA, Country Regulatory Groups, Technical and Quality… more
    Sanofi Group (09/20/25)
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