- Veterans Affairs, Veterans Health Administration (Brockton, MA)
- …promoted to the full performance level without further competition when all regulatory , qualification, and performance requirements are met. Selection at a lower ... vaccination program is a requirement for all Department of Veterans Affairs Health Care Personnel (HCP). Qualifications Basic Requirements: United States… more
- Veterans Affairs, Veterans Health Administration (Bedford, MA)
- …vaccination program is a requirement for all Department of Veterans Affairs Health Care Personnel (HCP). Qualifications Applicants pending the completion of ... or supervised practice program and provide a verification statement from the program director that conveys eligibility to take the CDR registration exam as a… more
- Rhythm Pharmaceuticals (Boston, MA)
- …or related field + 8+ years of highly relevant pharmaceutical/biotechnology experience in Regulatory Affairs Operations + Knowledge and understanding of the drug ... and our tenacity to overcome barriers, together. Opportunity Overview The Associate Director (AD) of Regulatory Operations is responsible for assisting the… more
- Takeda Pharmaceuticals (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as Director , Global Regulatory Labeling Strategy where you will be responsible for ... and assures that Takeda labeling content and processes conform to regulatory requirements. **Management of Local Exceptions and LOC Interactions** + Manages… more
- Sanofi Group (Cambridge, MA)
- …+ Collaborate with glocal cross-functional teams including Medical TA, Clinical Development, Regulatory Affairs , HEVA, Market Access, and Commercial to align ... **Job title** : Global Medical Director , Evidence Generation - Innovation & Partnerships **Location:**...engagement. We serve as key strategic partners for commercial, regulatory , R&D, market access and external affairs … more
- Grifols Shared Services North America, Inc (Fall River, MA)
- …for the therapeutic area(s). + Partners with the Medical Directors, National MSL Sr Director , and North America Medical Affairs Sr Director to develop ... and regions. The primary responsibility of the MSL Field Director is the management, performance, and coaching of a...of field medical plans, strategy, and activities within Medical Affairs , as aligned with goals and objectives. This position… more
- Sanofi Group (Cambridge, MA)
- …within the Sanofi portfolio of products. The team is part of the Global Regulatory Affairs , Regulatory CMC and Device Department within Global Research ... **Job Title:** GRA Device Lead ( Director ) **Location** : Morristown, NJ, Cambridge, MA, Framingham,...and Development. Sanofi's global regulatory affairs (GRA) function is comprised of… more
- Takeda Pharmaceuticals (Lexington, MA)
- …program management experienced in leading cross-functional clinical programs within Medical Affairs , Clinical Research, Regulatory , CMC or other drug development ... phases of development with significant experience within related functions (eg, Medical Affairs , Clinical Operations, Regulatory , CMC, Marketing). + Minimum of 5… more
- Philips (Cambridge, MA)
- …including Medical Affairs , Clinical Development, Research & Development, and Regulatory Affairs . + **Develops** clinical evidence strategies for New Product ... The Director Medical Writing & Clinical Development is a...a key member of the Ultrasound Medical and Clinical Affairs team and serves as a subject matter expert,… more
- Chiesi (Boston, MA)
- …and rewarding work. Who we are looking for Purpose As the Senior Director , Global Scientific Engagement and Innovation, you will spearhead the strategy, development, ... narratives for global stakeholders. + Partner with R&D, clinical development, regulatory , and commercial teams to ensure seamless, consistent messaging across all… more