- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …negotiations, and approval. + Review and propose continuous improvements to Global Labeling policies, end-to-end processes, quality , and system tools. ... across the organization to drive and align the development and maintenance of global labeling (eg CCDS, regional product labels, and patient labeling) for assigned… more
- Takeda Pharmaceuticals (Boston, MA)
- …grounded in purpose and be empowered to deliver your best. As part of the Global Medical Affairs Oncology team, you will report to the Head of Medical Excellence & ... the GMAO team and key cross-functional stakeholders such as Global Outcomes Research, and be a key contributor to...address those needs + Lead development and updating of high- quality medical affairs education and training plans and materials… more
- Takeda Pharmaceuticals (Boston, MA)
- …is true to the best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical & Quality Process Compliance is responsible for ... improvement that are enterprise-wide (ie Veeva, QMS, Enterprise Audit, etc.) to Global Quality and R&D Quality . Present to CPMQ at periodic intervals… more
- Boston University (Boston, MA)
- ** ASSOCIATE DIRECTOR , STEWARDSHIP PROJECT MANAGEMENT, Development & Alumni Relations, Donor** **Job Description** ** ASSOCIATE DIRECTOR , STEWARDSHIP ... accessible and welcoming to all, and to advance BUs global leadership in research, scholarship, artistic creation, and professional...Donor Relations & Stewardship team is looking for an Associate Director who will serve as the… more
- Sanofi Group (Cambridge, MA)
- **Job Title:** Associate Director , Medical Value and Outcomes (Mid-Atlantic) **Location** : Remote/Field **About the Job** The Medical Value & Outcomes team ... oncology specialty community. This position reports to MVO, Regional Director - West and is a member of the Sanofi...North American Medical Affairs team. We are an innovative global healthcare company, committed to transforming the lives of… more
- Bristol Myers Squibb (Devens, MA)
- …work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director Stability is responsible for stability product strategy and ... preparation, review and approval of stability reports and regulatory filings. The Associate Director is responsible for leading high-performance technical team,… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- The Associate Director , Scientific Communications manages the execution of the core scientific and medical communications strategy for the relevant therapeutic ... Director , CNS Medical Communications Lead. **Key Responsibilities Include:** ** Global Scientific Communication Strategy** + Manage and deliver a comprehensive,… more
- Sanofi Group (Cambridge, MA)
- **Job Title:** Associate Director , Audit Readiness, Patient Support Services, OPIE **Location:** Morristown, NJ Cambridge, MA **About the Job** Join the team ... patients with some of the highest unmet needs. **The Associate Director , Audit Readiness** will report to...Quality and Compliance teams to ensure alignment with global standards and regulatory requirements. **Process Governance & SOP… more
- Sumitomo Pharma (Boston, MA)
- …of ** Associate Director , Regulatory Affairs (Oncology).** The Associate Director is part of the Global Regulatory Affairs (GRA) team based in the ... Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations...provides possible solutions and mitigation strategy + Ensures the quality and content of all submissions to Health Authorities… more
- Sanofi Group (Framingham, MA)
- **Job Title:** Associate Director -CMC BioDPDM **Location** : Framingham, MA As Associate Director within CMC BioDPDM, you'll have the opportunity to lead ... could turn the impossible into possible for millions. The Associate Director role is a key leadership...and Manufacturing. You will be part of leading a global team focused on fast-paced, high quality … more