- Daiichi Sankyo, Inc. (Bernards, NJ)
- …early/late-stage drug development experience ideally including time in role such as a Global Project Leader at Sr. Director level or equivalent requiredRelevant ... therapeutic experience and proven ability to learn new indications requiredProven global line management expertise; experience of performance management and… more
- Capital One (Wilmington, DE)
- … Management experience At least 10 years of experience in project, risk program , Cloud risk management , or process managementAt least 10 years of experience ... Director , Business Risk Guide- Enterprise Services Risk OfficeWe...hiring! The Enterprise Services Business Risk Office provides risk management support to several lines of business including: Brand,… more
- Takeda Pharmaceutical (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide.The Associate Director Global Regulatory Affairs, Neuroscience is responsible for developing ... Global Regulatory Teams (GRTs) and representing the regulatory function on cross-functional Global Program Teams. Defines, develops, and leads global … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Human Resource Information System (HRIS) team to define / implement program functionality requirements for global HRISEmployee Experience:Develop, recommend and ... diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi...role includes DSE, DSI, DSJ, and may include other regions/ management units as needed to reflect changes to the… more
- Takeda Pharmaceutical (Boston, MA)
- … Global Regulatory Teams (GRTs) and representing the regulatory function on cross-functional Global Program Teams. The Senior Director also will lead ... appropriate R&D.Defines, develops, and leads global strategies to maximize global regulatory success towards achievement of program objectives for complex… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and Human Resource Information System (HRIS) team to define/implement program functionality requirements for global HRISReporting and Improvement:Oversee ... diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi...Canada, United States and Japan and may include other regions/ management units as needed to reflect changes to the… more
- Takeda Pharmaceutical (Boston, MA)
- …possible in order to bring life-changing therapies to patients worldwide.The Associate Director , Global Regulatory Affairs Advertising and Promotion (GRA A&P) ... Review Lead is accountable for management of all assigned programs/products as the internal expert...to prescription medicine promotion.How you will contribute:As our Associate Director , Global Regulatory Affairs Advertising and Promotion… more
- Takeda Pharmaceutical (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide.Join Takeda as Director , Global Regulatory Labeling Strategy where you will be responsible ... Lead, coordinates the process to obtain labeling approval by Labeling Senior Management Cross-functional team ( Global Labeling Oversight Committee - GLOC)… more
- Takeda Pharmaceutical (Boston, MA)
- …/ Purpose: Defines, develops and leads global strategies to maximize global regulatory success towards achievement of program objectives for complex and/or ... and influencing the field as applicable.Provides leadership and development for other global regulatory leads responsible for the design and execution of global… more
- Takeda Pharmaceutical (Boston, MA)
- …to hold strategic conversations with Regulatory, R&D and enterprise stakeholders regarding global Information Management processes and systems and the regulatory ... true to the best of my knowledge.Job DescriptionOBJECTIVES/PURPOSE:Reporting to the Head, Global Regulatory Operations (GRO), the Head of Global Regulatory… more
