- Takeda Pharmaceuticals (Boston, MA)
- …bring life-changing therapies to patients worldwide. Join Takeda as Director, Global Regulatory Labeling Strategy where you will be responsible for the development ... alignment of the labeling strategy and labeling content. **Interface with Senior Management Cross-Functional Team (GLOC)** + In alignment with TAU/MPD Labeling… more
- Eversource Energy (Westwood, MA)
- …visas for this position\._ **Our Team** Eversource is looking for a ** Senior Program Manager, Strategic Project Development, Transmission** located in ... and budgets in the conceptual phase prior to execution + Interacts regularly with Regulatory Affairs , Environmental Affairs , and Energy Efficiency to develop… more
- Sanofi Group (Cambridge, MA)
- **Job Title:** Senior Medical Science Liaison - Southeast **Location:** Remote/Field **About the Job** **About Sanofi** : We are an innovative global healthcare ... Maintain effective and appropriate communication among internal stakeholders (Medical Affairs colleagues, Medical Information and Commercial Operations) while maintaining… more
- Highmark Health (Boston, MA)
- …This job is responsible for planning, designing, implementing, and maintaining the Compliance Program and its related policies to ensure the business acts within the ... parameters of federal and state laws, regulations, and regulatory guidance. The incumbent is also responsible for the administration, interpretation, and enforcement… more
- Takeda Pharmaceuticals (Boston, MA)
- …preferred. + 12+ years of experience in pharmaceutical/biotech industry, with 8+ years in regulatory affairs or R&D operations. + Proven track record of leading ... and foster adoption of new initiatives. + Business Acumen: Strong understanding of regulatory affairs and enterprise strategy. + Analytical Thinking: Capable of… more
- Sanofi Group (Waltham, MA)
- …of the job/major challenges** + (S)He interacts with other GBS teams, Clinical, Regulatory , Global Program Head, Regulatory , Immunology, Medical Writing, ... **Job Title:** Senior Project Biostatistics Lead- Vaccines **Location:** Waltham, MA...is accountable for all statistical aspects of clinical development/medical affairs plans, studies and submissions activities (when applicable), including… more
- Wolters Kluwer (Waltham, MA)
- …nurses, accountants, lawyers, and tax, finance, audit, risk, compliance, and regulatory sectors. We help professionals deliver deep impact when it matters ... across GBCM. + Manage vendor relationships and support GBCM program management and leadership team operations, including meeting facilitation, documentation,… more
- Pfizer (Cambridge, MA)
- **Role Summary** The Senior Director Internal Medicine (SD), individual contributor, will generate real-world evidence (RWE) and epidemiology (Epi) studies in ... for communications in writing and in presentations to internal stakeholders, regulatory authorities, medical professionals and others. The SD will be accountable… more
- Astrix Technology (Boston, MA)
- …+ Collaborate with cross-functional teams, including preclinical, clinical operations, and regulatory affairs , to integrate and execute clinical strategy. + ... ** Senior Medical Director** Clinical Boston, MA, MA, US...lead the clinical development execution for their cardiovascular therapeutic program . This is a great chance to join a… more
- Takeda Pharmaceuticals (Boston, MA)
- …with functional experts across the R&D organization, such QS, Research, Biostatistics, Regulatory Affairs , DMPK, Pharm Sci, and Clinical Science providing ... company that will inspire you and empower you to shine? Join us as Senior Director, Quantitative Clinical Pharmacology Lead in our Cambridge, MA office. At Takeda,… more
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