- Sanofi Group (Cambridge, MA)
- …bring hope to patients with some of the highest unmet needs. Sanofi is recruiting a Director , US Medical Affairs . The Director will report to the Head of ... **Job Title:** US Medical Director , Dupilumab Atopic Dermatitis **Location:** Cambridge, MA /...US Medical Affairs , Dermatology. This position is based in Cambridge, MA… more
- Otsuka America Pharmaceutical Inc. (Waltham, MA)
- …but not limited to Translational Research & Biomarkers, Clinical Management, Global Regulatory Affairs , Global Clinical Development (late phase), Data & ... **Job Summary** The Senior Director will serve as the Translational Medicine CNS Therapeutic Area Head, reporting to the VP, Translational Medicine and Early… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …including INDs, IBs, clinical study reports, and NDAs/BLAs. + Collaborate with regulatory affairs on interactions with global health authorities. + Provides ... with emphasis on the large global clinical trials and regulatory filing activities. The Senior Director , GCD...trials and regulatory filing activities. The Senior Director , GCD is responsible for all the clinical development… more
- Sanofi Group (Cambridge, MA)
- …Research Director , Safety Officer and Pharmacovigilance, Translational Medicine, Regulatory Affairs , Biostatistics, Clinical Study Units, Medical Affairs ... **Job Title:** Development Scientific Director (DSD) **Location:** Cambridge, MA, **About the Job**...to the protocol development, study feasibility and risk assessment, regulatory submissions, protocol training, scientific review of data, and… more
- Sanofi Group (Cambridge, MA)
- …Development Plan (in close cooperation with other members of the team, particularly Regulatory Affairs and Health Economics); adjusts and updates the strategy ... **Job Title:** Senior Clinical Research Director **Location:** Morristown, NJ Cambridge, MA **About the...in the project in collaboration with the Safety Officer, Regulatory Strategist, Statistics and other key functional representatives to… more
- Philips (Cambridge, MA)
- …talented Hospital Patient Monitoring (HPM) CMO, the Clinical Development Portfolio Director is responsible for collaborating with multidisciplinary teams to deliver ... dissemination of evidence derived from clinical development endeavors, engaging with regulatory bodies and influential stakeholders to shape policy and industry… more
- State of Massachusetts (Boston, MA)
- …of Insurance ("DOI"), an Agency within the Office of Consumer Affairs and Business Regulation, administers the Commonwealth's insurance consumer protection laws ... their skills and talents to serve our citizens. *_About the Role:_* The Director of Pharmacy Benefit Manager Oversight operating within the Health Care Access Bureau… more
- Merck (Boston, MA)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …alignment with corporate quality objectives + Cross-functional Leadership:Collaborate with Regulatory Affairs , Technical Operations, Manufacturing, and Supply ... **Job Summary** The Associate Director , Global Product Quality - GMP Process is...preferred). + 8+ years of experience in pharmaceutical quality, regulatory affairs , or technical operations. + Proven… more
- Takeda Pharmaceuticals (Boston, MA)
- …functions across Takeda Oncology including Translational Medicine, Clinical Sciences, Global Regulatory Affairs , the Oncology Business Unit (Commercial and ... and empower you to shine? Join us as a Director , Global Program Management in our Cambridge office. At...external diagnostic partners, and supporting health authority meetings and regulatory submissions (PMAs etc). This role will partner closely… more