- Takeda Pharmaceuticals (Boston, MA)
- …therapies to patients worldwide. Join Takeda as an Senior Manager , Global Regulatory Affairs , CMC Small Molecules where you will oversee the ... recognizes and contributes to enhancing business processes. As part of the Global Regulatory Affairs CMC team, you will report to the Senior Director Global… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …and biomarker assay development and validation. + Collaborate with Global Manufacturing, Regulatory Affairs , and Global Quality to explore methods and implement ... empower you to shine? Join us as a Senior Manager of Statistics- CMC in our Cambridge,...as appropriate in a timely manner. + Respond to regulatory questions that are statistical in nature. + Increase… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …with 5+ years' experience or Master's degree with 2 years' experience in regulatory affairs or related areas (eg, clinical development, project management, ... needed. - Works collaboratively with members of the global regulatory team (GRL, regional leads, CMC -RA, labeling,...the global regulatory team (GRL, regional leads, CMC -RA, labeling, medical writing, regulatory operations, etc.)… more