- Takeda Pharmaceuticals (Boston, MA)
- …launch readiness for high-impact oncology programs. **How you will contribute:** + Lead global regulatory strategy for assigned programs across development ... medicines and make a lasting impact on patients worldwide. Join Takeda as a Senior Director, Global Regulatory Lead - Oncology, where you will be part of the … more
- Takeda Pharmaceuticals (Boston, MA)
- …Director, Global Regulatory Lead Oncology, you will define and lead global regulatory strategies for oncology programs, oversee major submissions, and ... treatments to patients globally. **How you will contribute:** + Define, develop, and lead global strategies to maximize global regulatory success towards… more
- Sanofi Group (Cambridge, MA)
- …with cross-functional teams, including medical leads, global study lead , statisticians, clinical supply managers, regulatory affairs specialists, etc. + ... **Job Title:** AI-Enabled Global Study Data Leader **Location:** Morristown,...commitment to accelerate the development of new drugs and medical devices for all patients through our clinical trials.… more
- Sanofi Group (Cambridge, MA)
- …Effectiveness (MO&E) and country teams. + Lead the execution of assigned medical affairs studies (EAP). Provide input in design, monitoring, analysis, and ... **Job Title:** Global Medical Director, Riliprubart **Location:** Cambridge,...miracles of science to improve people's lives", Specialty Care Medical Affairs have a vision to be… more
- Bristol Myers Squibb (Cambridge, MA)
- …strategy) understanding the relationship to clinical trial design. + In partnership with Medical Affairs , supports development of KOL plans and engagements, and ... and in their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** Global Program Leads within the ICV Global Program Leadership… more
- Bristol Myers Squibb (Cambridge, MA)
- …due diligence and business development assessments. + Working with regional regulatory staff as Global Regulatory Lead and US Regional Regulatory Lead on ... + 8-12 years pharmaceutical industry experience, including 6-8 years in regulatory affairs . Global experience strongly preferred with command of US experience… more
- Takeda Pharmaceuticals (Boston, MA)
- …medicines and make a lasting impact on patients worldwide. Join Takeda as a Director, Global Regulatory Lead Oncology where you will be part of the global ... regulatory team. As Director, Global Regulatory Lead Oncology you will set global regulatory strategy and lead major submissions for high-impact… more
- Sanofi Group (Cambridge, MA)
- …care + Experience collaborating with cross-functional groups, including Marketing, Sales, Medical Affairs , Market Research, Finance, Forecasting, Development + ... **Job Title:** Global Indication Lead , Rilzabrutnib IgG4, Rheumatology TA, Immunology Franchise **Location:** Cambridge, MA **About the Job** Join the team… more
- Takeda Pharmaceuticals (Boston, MA)
- …among functions represented at the Labeling cross functional teams including clinical, safety, medical affairs , and commercial, to ensure the highest level of ... therapies to patients worldwide. Join Takeda as Associate Director, Global Labeling Lead where you will be...US based employees may be eligible to participate in medical , dental, vision insurance, a 401(k) plan and company… more
- Sanofi Group (Cambridge, MA)
- **Job title** : Global Medical Director Hemophilia **Location:** Cambridge, MA / Morristown, NJ **About the job** The role reports to the Global Head of ... Hemophilia within the Global Medical Rare Disease Organization. Sanofi Rare Diseases has built...Market Access, HEVA/RWE, and Patient Advocacy. + Organize and lead medical insight gathering activities (eg, advisory… more