- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …business development programs. + Build professional network with key stakeholders outside of Global Regulatory Affairs to identify regulatory ... Description** + Oversee the capture, review, and dissemination of global regulatory news, public commenting opportunities, new...technical discipline preferred. + Minimum of 5 years of regulatory affairs experience. + Minimum 2-3 years'… more
- Sanofi Group (Cambridge, MA)
- **Job Title:** Global Medical Director , Riliprubart **Location:** Cambridge, MA **About the Job** Join the team transforming care for people with immune ... engagement. We serve as key strategic partners for commercial, regulatory , R&D, market access and external affairs ...and communication of the assigned studies. Serve as a global medical point of contact for such studies for… more
- Sanofi Group (Cambridge, MA)
- **Job Title:** Global Medical Director **Location** : Cambridge, MA **About the Job** Join the team transforming care for people with immune challenges, rare ... the Frexalimab strategy at the GBT level. + Participate and contribute to the Global Medical Affairs Strategic Plans for Frexalimab in line with key Strategic… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …documents, including INDs, IBs, clinical study reports, and NDAs/BLAs. + Collaborate with regulatory affairs on interactions with global health authorities. ... on the large global clinical trials and regulatory filing activities. The Senior Director , GCD...trial implementation and management. + Complete understanding of the global regulatory requirements. + Working knowledge of… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …Actions (CAPA), Deviations, and Change Control** , ensuring compliance with global regulatory requirements and internal standards. The successful candidate ... **Job Summary** The Associate Director , Global Product Quality - GMP...alignment with corporate quality objectives + Cross-functional Leadership:Collaborate with Regulatory Affairs , Technical Operations, Manufacturing, and Supply… 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
- 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)
- …+ Appropriately escalates issues to Global Labeling management and the Global Regulatory Lead (GRL) and proposes risk mitigation strategies for assigned ... life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will...+ Working within Labeling Team and GRA + Represents Global Labeling at Global Regulatory … more
- Takeda Pharmaceuticals (Boston, MA)
- …to the best of my knowledge. **Job Description** **About the role:** The Director , Global Medical Communications, Immunology, is a dynamic, strategic role within ... Global Medical Affairs responsible for driving the...review process for medical materials; Work with Legal and Regulatory colleagues to resolve questions and provide leadership in… more
- Bristol Myers Squibb (Cambridge, MA)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** Global Program Leads within the ICV Global Program Leadership ... late-stage challenges (eg, trends in disease area therapeutic advances, and evolving regulatory , patient advocacy and market access environments) to create a vision… more