- Takeda Pharmaceuticals (Cambridge, MA)
- …Pharmacometrics, Statistics, Drug Safety, Clinical Sciences, Outcomes, Digital Health, Pharmaceutical Sciences/Device, and Global Regulatory Affairs. + Advanced ... drive a MIDD path within each At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …in our Cambridge, MA office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. ... (US/EU/Japan/China) clinical development taking into consideration the medical, scientific, regulatory and commercial issues for assigned Takeda pipeline compounds.… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …team on a high priority molecule. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. ... (US/EU/Japan) clinical development taking into consideration the medical, scientific, regulatory and commercial issues for assigned Takeda pipeline compounds. +… more
- Takeda Pharmaceuticals (Lexington, MA)
- …lead a team to ensure analytical methods and strategies meet scientific, regulatory , and quality standards necessary for regulatory filings, commercial ... and lifecycle management. You will work within a collaborative, cross-functional Pharmaceutical Sciences team, contributing to program strategies and applying your… more
- Sumitomo Pharma (Boston, MA)
- …and aggregate safety reports + Knowledge of drug development in the pharmaceutical industry, including clinical research and global regulatory requirements + ... Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations...Safety Charters + Handles Health Hazard Evaluations and Ad-Hoc Regulatory safety inquiries. + Represents PVRM on post-marketing product… more
- Norstella (Boston, MA)
- …on clinical trials, drug treatments, medical devices and what's new in the regulatory and commercial landscape. Relying on us to deliver vital advantage when making ... our customers come from over 3000 of the world's leading pharmaceutical , contract research organizations (CROs), medical technology, biotechnology and healthcare… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …will be recognized as a technical resource/expert within SMPD and across Pharmaceutical Sciences and utilize their technical expertise to contribute across multiple ... analytical development, drug product development, manufacturing, quality assurance, and regulatory affairs, to develop and implement effective process engineering… more
- Sumitomo Pharma (Boston, MA)
- Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... and vendors, and ensures the documentations are in accordance with GCP regulatory requirements and consistent with the protocol for assigned studies. + Participates… more
- State of Massachusetts (Boston, MA)
- …prescription drug manufacturers, and of their disclosure practices in relation to regulatory standards and statutory requirements. * Manage the review of pharmacy ... external stakeholders to explore pharmacy benefit policy issues and develop regulatory guidance where appropriate. * Provide technical assistance in the development… more
- Sumitomo Pharma (Boston, MA)
- Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... but not limited to, Clinical Development, Translational Medicine/Early Development, Regulatory Affairs, Data Management and Biostatistics is essential. **Job Duties… more