- Bristol Myers Squibb (Cambridge, MA)
- …digital health and other devices to enhance the value of our pharmaceutical products across therapeutic areas + Responsible for understanding the regulatory ... assessing regulatory risk, and developing global filing strategies. + Co-lead marketing application submission teams for indications that are at regulatory filing… more
- J&J Family of Companies (Raynham, MA)
- …WW. This includes Research & Development, Clinical, Regulatory, Marketing , Sales, Manufacturing, Procurement, Information Management, Communications ... degree desired + Minimum 15 years of experience in a medical device, pharmaceutical or similar regulated industry, 10 years of which are at management level,… more
- Sanofi Group (Cambridge, MA)
- …generated by the company in collaboration with the Global Neurology Medical Communications Director, internal contributors, and agencies. + Ensure that they and ... support, education, and guidance to US and Global Neurology Commercial Marketing , Sales, & Market Access teams. Support will include presentations, representative… more
- Takeda Pharmaceuticals (Boston, MA)
- …in a scientific discipline (PharmD/PhD/MD) strongly preferred + 12+ years of pharmaceutical industry experience. This is inclusive of 10 years of regulatory ... process and regulatory requirements. Knowledge of FDA, EU, Canada, ROW and post- marketing a plus. + Understand and interpret complex scientific issues across… more
- Takeda Pharmaceuticals (Boston, MA)
- …**Requirements/Qualifications:** + BSc Degree, preferred. BA accepted. + 8+ years of pharmaceutical industry experience. This is inclusive of 6 years of regulatory ... process and regulatory requirements. Knowledge of FDA, EU, Canada, ROW and post- marketing a plus. + Understand and interpret complex scientific issues across… more
- Takeda Pharmaceuticals (Boston, MA)
- …in a scientific discipline (PharmD/PhD/MD) strongly preferred + 8+ years pharmaceutical industry, inclusive of regulatory and/or related experience. + Preferred ... process and regulatory requirements. Knowledge of FDA, EU, Canada, ROW and post- marketing a plus. + Understand and interpret complex scientific issues across… more
- Norstella (Boston, MA)
- …of drug, device, company, clinical trial and market intelligence in the Pharmaceutical and MedTech markets. **Responsibilities** + Review, draft, and negotiate a ... agreements, consulting and professional services agreements, master services agreements, marketing and advertising agreements, procurement contracts and other complex… more