- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …with 5+ years' experience or Master's degree with 2 years' experience in regulatory affairs or related areas (eg, clinical development, project management, ... needed. - Works collaboratively with members of the global regulatory team (GRL, regional leads, CMC -RA, labeling,...the global regulatory team (GRL, regional leads, CMC -RA, labeling, medical writing, regulatory operations, etc.)… more
- Takeda Pharmaceuticals (Lexington, MA)
- …Clinical Research and program management experience working with clinical programs within Medical Affairs , Clinical Research, Regulatory , CMC or other drug ... **Job Description** The objective and purpose of the Senior Manager , US Medical Clinical Research, RPE position is as...trials in assigned TA. Ensure coordination with Pharmacovigilance and Regulatory Affairs to respond to external audits… more
- Takeda Pharmaceuticals (Lexington, MA)
- …and program management experienced in leading cross-functional clinical programs within Medical Affairs , Clinical Research, Regulatory , CMC or other drug ... phases of development with significant experience within related functions (eg, Medical Affairs , Clinical Operations, Regulatory , CMC , Marketing). + Minimum… more