- Takeda Pharmaceuticals (Boston, MA)
- …therapies to patients worldwide. The Associate Director Global Regulatory Affairs , Neuroscience is responsible for developing innovative global regulatory strategies ... appropriate regulatory strategy. + Participates in cross-functionalinitiativeswithin Global Regulatory Affairs and Takeda R&D. **How you will contribute:** + The… more
- Sanofi Group (Cambridge, MA)
- …labeling leadership to cross-functional teams (Regulatory Strategy, Clinical Development, Medical Affairs , Pharmacovigilance, Market Access ). + Contribute ... **Job Title:** Director, Global Regulatory Affairs - Global Labeling Strategy **Location** : Morristown,...field. + Minimum 10 years of experience in the pharmaceutical or biotechnology industry, including 5-6 years in regulatory… more
- Rhythm Pharmaceuticals (Boston, MA)
- …to overcome barriers, together. Opportunity Overview In the Associate Director, Regulatory Affairs role, you will be responsible for ensuring the development and ... for your assigned programs. By joining our growing and dynamic regulatory affairs team, you'll be responsible for the effective management and timely execution… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …of the global regulatory team (GRL, regional leads, CMC-RA, labeling, medical writing, regulatory operations, etc.) to develop global regulatory plans, address ... Skills, and Competencies** **K** **nowledge** - Experience working in the pharmaceutical and/or healthcare industry. - Knowledge and experience with preparation of… more
- Sanofi Group (Cambridge, MA)
- …year (3+ years preferred) of regulatory experience, preferably within the pharmaceutical / medical device/biotech industry + Knowledge and understanding of complex ... **Job Title:** Associate Director, Global Regulatory Affairs Advertising and Promotion **Location** : Cambridge, MA Morristown, NJ **About the Job** Are you ready to… more
- Takeda Pharmaceuticals (Boston, MA)
- …registration strategies. You will be RA CMC member on Regulatory, Pharmaceutical Development, and Production project teams throughout clinical development and ... enhancing business processes. As part of the Global Regulatory Affairs CMC team, you will report to the Senior...a Scientific Discipline, Advanced Degree preferred. + 8+ years pharmaceutical Regulatory CMC experience including experience as an RA… more
- Takeda Pharmaceuticals (Boston, MA)
- …life-changing therapies to patients worldwide. Senior Associate - Specialist, Global Regulatory Affairs CMC role is within in the GRA Chemistry Manufacturing & ... for assigned products. + Support RA CMC member on Regulatory, Pharmaceutical Development, and Commercial project teams throughout clinical development and commercial… more
- Takeda Pharmaceuticals (Boston, MA)
- …in a scientific discipline (PharmD/PhD/MD) strongly preferred + 6+ years of pharmaceutical industry experience. This is inclusive of 4+ years of regulatory ... of regulatory strategy such as understanding broad concepts within regulatory affairs and implications across the organization and globally; proactively identifies… more
- Takeda Pharmaceuticals (Boston, MA)
- …life-changing therapies to patients worldwide. The Senior Global Regulatory Affairs , Neuroscience is responsible for developing innovative global regulatory ... BA acceptable with significant Industry experience. + Sr Director 12+ years of pharmaceutical industry experience inclusive of 10 years of regulatory experience or a… more
- Veterans Affairs, Veterans Health Administration (Leeds, MA)
- …Healthcare System's catchment area. The Chief provides leadership needed to provide pharmaceutical care and medication therapy management to all patients served by ... change and unites employees in pursuit of patient focused pharmaceutical care objectives. The Chief, Pharmacy Service holds a...in Leeds, CWM HCS is a complex 130 bed medical center with a highly diverse patient population in… more