• Associate Director , Global…

    Takeda Pharmaceuticals (Boston, MA)
    …transformative medicines and make a lasting impact on patients worldwide. Join Takeda as Associate Director , Global Regulatory Lead Oncology where you will ... be part of the global regulatory team. As Associate Director ,...classified as "hybrid" following Takeda's Hybrid and Remote Work policy . \#LI-Hybrid \#LI-AA1 **Takeda Compensation and Benefits Summary** We… more
    Takeda Pharmaceuticals (10/30/25)
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  • Associate Director , Global…

    Takeda Pharmaceuticals (Cambridge, MA)
    …is possible in order to bring life-changing therapies to patients worldwide. The Associate Director , Global Regulatory Affairs Advertising and Promotion (GRA ... pertaining to prescription medicine promotion. **How you will contribute:** + As our Associate Director , Global Regulatory Affairs Advertising and Promotion… more
    Takeda Pharmaceuticals (10/29/25)
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  • Associate Director

    Sumitomo Pharma (Boston, MA)
    …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate Director , Regulatory Affairs (Oncology).** The Associate ... Director is part of the Global Regulatory Affairs (GRA) team based in the US. He/She...in line with your work state. Our robust time-off policy includes flexible paid time off, 11 paid holidays… more
    Sumitomo Pharma (10/11/25)
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  • Associate Director , Global…

    Takeda Pharmaceuticals (Boston, MA)
    … strategies in collaboration with their regional counterparts. **Accountabilities:** + The Associate Director will be responsible for complex or highly complex ... + Defines, develops and leads global strategies to maximize global regulatory success towards achievement of program objectives for complex and/or multiple… more
    Takeda Pharmaceuticals (11/11/25)
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  • Regulatory Affairs Associate

    GRAIL (Boston, MA)
    …filings. + Manage the creation and review of Standard Operating Procedures and policy guidelines within the regulatory affairs department. + Perform other duties ... For more information, please visit grail.com . The role assists with regulatory strategy and the development of submissions in partnership with key internal… more
    GRAIL (12/03/25)
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  • Associate Medical Director

    Takeda Pharmaceuticals (Cambridge, MA)
    …will inspire you and empower you to shine? Join us as an Associate Medical Director , Clinical Science, Neuroscience- Pulmonologist/Neurologist in our Cambridge, ... be a vital contributor to our inspiring, bold mission. **POSITION OBJECTIVES:** The Associate Medical Director leads and drives strategy for the overall global… more
    Takeda Pharmaceuticals (10/23/25)
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  • Associate Director , Biostatistics

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …needs and nutraceutical products for the maintenance of everyday health. As an Associate Director , Biostatistician, you will be a champion of Otsuka's culture ... in the drug development including clinical development plan and regulatory submission strategy. This is a strategic and critical...can also be considered. Otsuka maintains a hybrid work policy and travel is expected 20% of the time… more
    Otsuka America Pharmaceutical Inc. (12/03/25)
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  • Associate Director , Scientific…

    Takeda Pharmaceuticals (Boston, MA)
    …the development of scientific communications strategy and deliverables, the ** Associate Director , Scientific Communications Lead, Hematology** proactively ... preferably in life sciences, and excellent project management skills. The Associate Director , Scientific Communications Lead, develops and implements strategic… more
    Takeda Pharmaceuticals (12/11/25)
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  • Associate Medical Director

    Sumitomo Pharma (Boston, MA)
    …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate ** **Medical Director , Clinical Development - Oncology** . The ... associate medical director is responsible for the leadership, development, and management...strong medical and scientific principles, knowledge of compliance and regulatory requirements, markets, business operations, and emerging issues. +… more
    Sumitomo Pharma (11/15/25)
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  • Associate Director , OHRS

    Dana-Farber Cancer Institute (Brookline, MA)
    The Associate Director , Office for Human Research Studies (OHRS), oversees operational activities supporting IRB review and human research protections across the ... the Director to ensure consistency across the DF/HCC consortium. ** Policy , SOPs, and Quality:** Lead development, maintenance, and communication of OHRS SOPs… more
    Dana-Farber Cancer Institute (01/02/26)
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