• Director , Quantitative Clinical…

    Takeda Pharmaceuticals (Cambridge, MA)
    …Drug Safety, Clinical Sciences, Outcomes, Digital Health, Pharmaceutical Sciences/Device, and Global Regulatory Affairs . + Advanced knowledge of regulatory ... you and empower you to shine? Join us as Director , Quantitative Clinical Pharmacology (QCP) Lead in our Cambridge,...a MIDD path within each project. + Leads strategic, scientific , and operational aspects of multiple drug development projects… more
    Takeda Pharmaceuticals (09/25/25)
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  • Field Medical Outcomes, Director , MD

    Pfizer (Boston, MA)
    …to achieve Medical objectives (b) Understand the priorities of Pfizer Medical Affairs in order to contribute to Medical educational content strategy development and ... and other Pfizer Field Medical colleagues (d) Demonstrate expertise in scientific communication across multiple channels, including, but not limited to, live… more
    Pfizer (10/02/25)
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  • Senior Director , Quantitative Clinical…

    Takeda Pharmaceuticals (Boston, MA)
    …with functional experts across the R&D organization, such QS, Research, Biostatistics, Regulatory Affairs , DMPK, Pharm Sci, and Clinical Science providing ... contributor to our inspiring, bold mission. **Position Objectives:** + The Senior Director manages strategic, scientific and operational aspects of multiple… more
    Takeda Pharmaceuticals (09/11/25)
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  • Global Medical Director - Hemophilia

    Sanofi Group (Cambridge, MA)
    …management, politically astute and role model teamwork and collaboration. + Highest ethical, regulatory and scientific standards. **Why Choose Us** + Bring the ... **Job title** : Global Medical Director Hemophilia **Location:** Cambridge, MA / Morristown, NJ...+ Accountable for implementing stakeholder engagement, medical education, and scientific communication plans aligned with the strategic priorities of… more
    Sanofi Group (09/12/25)
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  • Associate Director , Global Regulator…

    Bristol Myers Squibb (Cambridge, MA)
    …(Masters, PhD, PharmD, BSN, etc.) with at least 3+ years of Regulatory Affairs experience in the pharmaceutical industry. **Key Competency Requirements** ... in their personal lives. Read more: careers.bms.com/working-with-us . **Associate Director , Global Regulatory Strategy, Neuroscience** **Position Summary:** The… more
    Bristol Myers Squibb (08/28/25)
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  • Director , Pharmaceutical Sciences Program…

    Takeda Pharmaceuticals (Boston, MA)
    …analytical/organic/physical chemistry, process engineering, pharmaceutics, quality assurance and/or regulatory affairs . Advanced understanding in DMPK, ... global initiatives **Accountabilities:** **Program Leadership** **:** + Provides strategic scientific leadership and program management for multiple global CMC… more
    Takeda Pharmaceuticals (09/25/25)
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  • Senior Medical Director

    Astrix Technology (Boston, MA)
    …+ Collaborate with cross-functional teams, including preclinical, clinical operations, and regulatory affairs , to integrate and execute clinical strategy. + ... **Senior Medical Director ** Clinical Boston, MA, MA, US Pay Rate...Ensure clinical initiatives are aligned with organizational goals and scientific advancements. + Design and direct early-phase clinical trials,… more
    Astrix Technology (08/11/25)
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  • Associate Director , Global Neurology…

    Sanofi Group (Cambridge, MA)
    …role includes strategic development and execution of clinical data and regulatory milestones; congress and publication communications; scientific platform ... scientific data aptitude with experience managing product and regulatory milestone communications independently + Expertise in communications concepts, practices,… more
    Sanofi Group (09/20/25)
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  • Director , Global Integrated Evidence…

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …Early Phase & Translational Medical, Clinical Development, Value and Real-World Evidence, Regulatory , Medical Affairs , Data and Analytics, Digital Health and ... evidence generation strategy, operational excellence and digital innovation. The Director , Global Integrated Evidence Strategy is an important leadership position… more
    Otsuka America Pharmaceutical Inc. (09/13/25)
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  • Principal Medical Director , Product…

    Genentech (Boston, MA)
    … will have strong collaboration with cross-functional teams, including clinical research, regulatory affairs , and product development, to ensure the successful ... join the Cardiovascular, Renal, and Metabolism group. The role of Principal Medical Director will focus on guiding the development of our CVRM portfolios. The ideal… more
    Genentech (09/12/25)
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