- Takeda Pharmaceuticals (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide. As Associate Director , Global Labeling Devices, you will be responsible for the development, ... to provide input into Clinical IFU, design input requirements, quality system required documentation, human factors strategy, and regulatory strategy.… more
- Takeda Pharmaceuticals (Boston, MA)
- …life cycle activities across the portfolio of PDT products. The Global Regulatory Lead, Director , in PDT R&D: + Serves as the global regulatory lead for one or ... cross-functional sub teams and working groups. + Creates high quality , complaint regulatory documents (eg, BLAs, INDs, CTAs, MAAs,...plus. BA accepted + Minimum of 10 years of pharmaceutical industry experience, with a minimum of 8 years… more
- Sanofi Group (Cambridge, MA)
- **Job Title:** Global Medical Affairs Senior Director , Gastroenterology **Location:** Cambridge, MA / Morristown, NJ **Hiring Manager:** Cristina Almansa **About The ... in Academia and/or industry. + Strong understanding of the pharmaceutical /biotech drug development and commercialization process. + Excellent communication and… more
- Sanofi Group (Cambridge, MA)
- **Job Title:** Senior Director , Neurology and Immunology HEVA Business Partner **Location:** Cambridge, MA **About the Job** Sanofi's specialty care business unit ... + Understanding of the legal and regulatory environment of the pharmaceutical industry, demonstrated integrity on work-related compliance considerations and solid… more
- Sanofi Group (Waltham, MA)
- **Job Title:** Statistical Project Leader, Deputy Director , Global Biostatistics Sciences **Location** : Waltham, MA **About the Job** Are you ready to shape the ... Earned PhD in statistics or related discipline with 2+ years of applicable pharmaceutical or biotech experience, OR earned Master's degree with 5+ years of… more
- Lilly (Boston, MA)
- …and volunteerism. **Summary** We are looking for a proactive, scientifically grounded Director to lead the development and integration of GMP cell banking, ... media preparation, and formulation workflows. + Collaborate cross-functionally with Quality , Regulatory, Analytical Development, and Manufacturing (CDMOs) to support… more
- Takeda Pharmaceuticals (Boston, MA)
- …and plans to address those needs + Lead development and updating of high- quality medical affairs education and training plans and materials to drive a consistent ... certified as scientific experts on Takeda Oncology products + Collaborate with the Director of Heme-Onc and Pipeline Disease & Product Training to implement training… more
- Takeda Pharmaceuticals (Boston, MA)
- …Takeda is seeking a passionate and strategic leader for the role of Director , Dermatology HCP Marketing. This position is integral to the successful launch and ... and mission. + Hold internal teams and external agencies accountable for delivering quality work on time and within budget. + **Strategic Brand Leadership** : +… more
- Sanofi Group (Cambridge, MA)
- **Job Title:** Medical Affairs Director - Evidence Generation, Respiratory **Location:** Cambridge, MA Our Medical function serves as a valued strategic partner with ... academicians, in the scientific/medical arena. + Strong understanding of pharmaceutical /biotech clinical research. + Leadership skills: personal style that includes… more
- Sanofi Group (Cambridge, MA)
- …of what you thought was possible. Ready to get started? The Senior Clinical Research Director (Sr CRD) is noted as the **primary clinical lead for programs** . The ... (spoken and written) + At least 4 years in pharmaceutical industry or CRO, previous experience in clinical development...a wide range of health and wellbeing benefits including high- quality healthcare, prevention and wellness programs and at least… more