- Takeda Pharmaceuticals (Boston, MA)
- …with key functions across Takeda Oncology including Translational Medicine, Clinical Sciences, Global Regulatory Affairs , the Oncology Business Unit ... and empower you to shine? Join us as a Director , Global Program Management in our Cambridge...data integration. + Understanding of key considerations relevant to global regulatory requirements + Experience developing team… more
- Takeda Pharmaceuticals (Boston, MA)
- …Payer Marketing and Market Access, Global Evidence and Outcomes, Medica Affairs , Clinical Development, Regulatory Affairs , Biostatistics, Global ... Market Access, Pricing, Advocacy, Biostatistics, Global Evidence and Outcomes, Medical Affairs , Clinical Science, Legal, Regulatory + OBU 10, EUCAN, GEM… more
- Candela Corporation (Marlborough, MA)
- …potential improvement actions related feedback. . Jointly accountable with Quality System (QS) and Regulatory Affairs ( RA ) Leadership for ensuring the QS is ... **Sr. Director , Design and Supplier Quality** Requisition Number **2882**...regulatory / compliance. . Working understanding of relevant global /regional medical device regulations and standards with particular emphasis… more
- Takeda Pharmaceuticals (Boston, MA)
- …+ Manufacturing Sciences + Global Manufacturing Supply, Global Quality and Global Regulatory Affairs . + SME for Takeda drug product manufacturing ... DP/PKG** **Location: Cambridge, MA** **About the role:** As a Process Scientist (Associate Director ) - Global Manufacturing Science GMSci Drug Product (DP), you… more
- Olympus Corporation of the Americas (Westborough, MA)
- …applicable federal, state or local law. Posting Notes: || United States (US) || Massachusetts (US-MA) || Westborough || Quality & Regulatory Affairs (QA/ RA ) ... and governance supports business objectives through: proactive monitoring and application of global regulatory requirements within the regional QMS; leading the… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …study report (FSR), including authoring statistical sections. + Discusses strategies with Global Clinical Development and Regulatory Affairs regarding study ... team and key stakeholders across different functional areas such as clinical, regulatory affairs , asset management, safety and clinical operation. + Familiar… more
- Bristol Myers Squibb (Devens, MA)
- …Science and Technology, Business Process Management, Internal and External Manufacturing, Regulatory Affairs , Brand Teams, Legal, Patient Safety, Medical ... executed in strict adherence to applicable regulations and BMS standards. The Executive Director leads a team dedicated to maintaining global compliance across… more
- 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
- Sanofi Group (Cambridge, MA)
- …Development Plan (in close cooperation with other members of the team, particularly Regulatory Affairs and Health Economics); adjusts and updates the strategy ... **Job Title:** Senior Clinical Research Director **Location:** Morristown, NJ Cambridge, MA **About the...boards + Serves as clinical team leader/representative at the global project team(s), regulatory agency meetings, Steering… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …Statistics, Drug Safety, Clinical Sciences, Outcomes, Digital Health, Pharmaceutical Sciences/Device, and Global Regulatory Affairs . + Advanced knowledge of ... you and empower you to shine? Join us as Director , Quantitative Clinical Pharmacology (QCP) Lead in our Cambridge,... interactions. + Represents Clinical Pharmacology in meetings with global or regional regulatory agencies and be… more
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