- Takeda Pharmaceuticals (Boston, MA)
- …possible in order to bring life-changing therapies to patients worldwide. Join Takeda as a Senior Director , GRA Pharmaceuticals - Small Molecule where you ... Affairs CMC team, you will report to the Executive Director and Head, CMC Regulatory Affairs - Pharmaceuticals...**How you will contribute:** + Leads the Early Development Pharmaceuticals GRA CMC regulatory team in the… more
- Takeda Pharmaceuticals (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as a Director , GRA CMC Pharmaceuticals , Oligonucleotides where you will lead the ... GRA CMC Pharmaceuticals regulatory team in the development and implementation of..., Oligonucleotides team, you will report to the Executive Director and Head, CMC Regulatory Affairs, Pharmaceuticals .… more
- Takeda Pharmaceuticals (Boston, MA)
- …company that will inspire you and empower you to shine? Join us as a Senior Director , Global Regulatory Project Management, GI 2 within our Global Regulatory ... and Remote Work policy. **LOCATION & TRAVEL** + Remote within the US + Travel: The Director is expected to come to Quarterly GRA meetings in Cambridge & ad hoc… more
- Takeda Pharmaceuticals (Boston, MA)
- …partnering and/or investment. + In collaboration with Global Regulatory Affairs ( GRA ), monitor and communication with Takeda Oncology current and emerging regulatory ... At least 10 years experience in Business Development and Licensing within pharmaceutical or biotech sector, with focus on oncology, hematology or immuno-oncology. +… more
- Sanofi Group (Cambridge, MA)
- …GRA -Devices. Attends HA meetings and collaborates with the regions / GRA -CMC / GRA -Devices to communicate the outcome to senior management as needed + May ... in post-marketing activities required + At least 6 years of prior pharmaceutical /biotechnology industry experience, including at least 4 years of relevant Regulatory… more
- Sanofi Group (Cambridge, MA)
- …GRA -Devices. Attends HA meetings and collaborates with the regions / GRA -CMC / GRA -Devices to communicate the outcome to senior management as needed + May ... pre-marketing/development activities required + At least 6 years of prior pharmaceutical /biotechnology industry experience, including at least 4 years of relevant… more
- Sanofi Group (Cambridge, MA)
- …efforts. Reporting through Region North America within Global Regulatory Affairs ( GRA ), the candidate will work collaboratively with both internal and external ... stakeholders to identify areas important to Sanofi and pharmaceutical business, development of policy positions, creation and execution of advocacy strategies to… more