- Takeda Pharmaceuticals (Lexington, MA)
- …as an Associate Director , US Publications where you will work with Director , US Publications and assigned USM Product Medical Team(s) in developing and ... You will also have responsibility for supporting the development of assigned medical and scientific communication strategy and plans in collaboration with respective… more
- AbbVie (Boston, MA)
- …medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's ... in support of the overall Product Development Plan, based on strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's… more
- Pfizer (Cambridge, MA)
- …the clinical plans and clinical expertise are provided to project teams, including medical monitoring of clinical trials. + To support projects from Research to ... reviews and prepare summaries to support clinical development programs. + Medical resource for design and interpretation of clinical and preclinical programs… more
- Sanofi Group (Cambridge, MA)
- **Job Title:** Associate Director , Global Regulatory Affairs - Global Labeling Strategy **Location** : Morristown, NJ or Cambridge, MA (Hybrid) **About the Job** Are ... could be critical in helping our teams accelerate progress. The Associate Director , Global Regulatory Affairs - Global Labeling Strategy is responsible for leading… more
- Takeda Pharmaceuticals (Lexington, MA)
- …degree with 15+ years of experience** + Minimum 5 years of combination product, medical device, or pharmaceutical industry experience + Experience with both ... offers an exceptional opportunity to drive innovation at the intersection of medical devices and pharmaceutical development, with significant impact on patient… more
- Bristol Myers Squibb (Cambridge, MA)
- …medicine and R&D. We have an exciting opportunity for a Senior Director to join the Precision Medicine, Bioanalytical and Translational Sciences organization, where ... and Alliances in support of the BMS portfolio. **Summary:** The Senior Director of Precision Medicine Search, Evaluation, and Alliances is responsible for leading… more
- Takeda Pharmaceuticals (Boston, MA)
- …MSc, PhD, PharmD, MD). BA acceptable with significant Industry experience. + Sr Director 12+ years of pharmaceutical industry experience inclusive of 10 years ... the regulatory function on cross-functional Global Program Teams. The Senior Director also will lead discussions of regulatory strategy with senior leadership… more
- Sanofi Group (Cambridge, MA)
- **Job Title:** Director , Global Regulatory Affairs - Global Labeling Strategy **Location** : Morristown, NJ or Cambridge, MA (Hybrid) **About the Job** Are you ready ... Your skills could be critical in helping our teams accelerate progress. The Director , Global Regulatory Affairs - Global Labeling Strategy is responsible for leading… more
- Sanofi Group (Cambridge, MA)
- …Global Project Head, Research Scientist, Clinical Pharmacologist, Biomarker Lead, Safety Medical Director , Statistician, Regulatory and other key functional ... **Job Title:** Clinical Research Director **Location:** Cambridge, MA, **About the Job** Are...and diverse internal stakeholders and collaborators. + Evaluates relevant medical literature and status from competitive products. **Lead, support… 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**...R&D colleagues, as well as other stakeholders (eg, Legal, Medical , Marketing, Communications and Compliance). + Participates in the… more