• Manager , Regulatory Affairs

    Takeda Pharmaceuticals (Boston, MA)
    …Description** Takeda Development Center Americas, Inc. is seeking a Manager , Global Regulatory Affairs CMC in Cambridge, MA with the following ... requirements: Master's degree in Regulatory Affairs or related field plus 2 years of related experience. Prior experience must include: Develop the regulatory more
    Takeda Pharmaceuticals (03/28/24)
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  • Director, Regulatory Affairs

    Takeda Pharmaceuticals (Boston, MA)
    …order to bring life-changing therapies to patients worldwide. Join Takeda as a Director, Regulatory Affairs Vaccines CMC where you will provide program ... regulations and guidelines by applying interpersonal skills and expert Regulatory Affairs Vaccines (RAV) CMC ...to support their development + May serve as direct/matrix manager of RAV CMC staff, depending on… more
    Takeda Pharmaceuticals (04/18/24)
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  • Business Development Manager Oligo/Peptide

    WuXi AppTec (Boston, MA)
    …needs in TIDES drug development from discovery through clinical to commercial. Moreover, our Regulatory Affairs CMC team is experienced in preparing CMC ... drug). We greatly simplify the TIDES drug development by providing all discovery, CMC development and the entire manufacturing supply chain under one roof. With over… more
    WuXi AppTec (03/08/24)
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  • USA - Program Manager - Business…

    Randstad US (Cambridge, MA)
    …+ Knowledge of pharmaceutical industry and Project management experience within Medical Affairs , Clinical Research, Regulatory , CMC , Marketing or other ... usa - program manager - business professional. + cambridge , massachusetts...program level budgets across multiple projects + Knowledge of regulatory and compliance guidelines governing medical affairs more
    Randstad US (04/20/24)
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  • Vice President, Clinical Development

    Editas Medicine (Cambridge, MA)
    …significant clinical components and implications. + Collaborate closely with Non-clinical, Regulatory , Clinical Operations, CMC and Biometrics to ensure tight ... the clinical pipeline. The incumbent is expected to have a strong clinical, regulatory and scientific foundation, and will work closely with the cross functional… more
    Editas Medicine (03/07/24)
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