- Takeda Pharmaceuticals (Cambridge, MA)
- …the organizations mission, vision, scientific objectives and business goals + Collaborate with senior leaders to help integrate medical affairs into the overall ... of regulatory guidelines and compliance requirements relevant to medical affairs activities. + Proven leadership and people management skills and the ability… more
- Chiesi (Boston, MA)
- About us Based in Parma, Italy, Chiesi is an international research-focused pharmaceuticals and healthcare group with 90 years' experience, operating in 30 countries ... important and rewarding work. Who we are looking for Purpose As the Senior Director, Global Scientific Engagement and Innovation, you will spearhead the strategy,… 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
- Sanofi Group (Cambridge, MA)
- …Global Project Head (GPH) is delegated various responsibilities by the Senior GPH and/orTherapeutic Area Head to provide leadership, supervision, and coordination ... The GPH position requires achieving results through others and supporting the senior management team in achieving corporate goals. The GPH establishes the goals… more
- Deloitte (Boston, MA)
- …or public policy organizations, with preference for experience working on financial regulatory issues (audit, tax, trade) including with international bodies/ ... teams to perform in-depth analysis and provide compelling points of view to senior Deloitte leadership around the world. Your insights will contribute to unique and… more
- Takeda Pharmaceuticals (Boston, MA)
- …communicate safety issues with other functional areas such as Clinical Development, Regulatory Affairs , Quality Assurance, Medical Affairs , Marketing, ... management and/or risk management. + Knowledge and understanding of national and international PV and regulatory guidelines. **Travel Requirements:** Local and … more
- Catalent Pharma Solutions (Chelsea, MA)
- …of final products. **EDUCATION AND** **EXPERIENCE** : Requires a Bachelor's degree in Drug Regulatory Affairs and 4 years of experience in job offered or 4 ... Perform various quality assurance checks during all manufacturing processes; Assess regulatory and quality risks in manufacturing activities and processes according… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …+ Leads flagships medical programs as defined by the Global Medical Affairs (GMA) Strategy Team and sub-teams + Leads GMA-driven evidence generation, taking ... into consideration the medical, scientific, regulatory and commercial considerations + Supports multi-disciplinary matrix teams...as a study Medical Lead for the GMA Medical Affairs Company Sponsored / Collaborative studies + Manages complex… more
- Sanofi Group (Cambridge, MA)
- …senior scientific, technical, finance, commercial, medical, market access, industrial affairs , regulatory and other functional representatives to develop ... development and execution + Build and present clear, compelling recommendations to senior management leveraging expertise in visual tools (PPT, etc.) + Manage… more
- GE HealthCare (Boston, MA)
- … leadership + Collaborate cross-functionally within PDx clinical study teams, with medical affairs and product leaders + Travel to international and domestic ... + Author and review imaging sections of trial-facing and regulatory documents + Collaborate with R&D Digital colleagues in...**Qualifications** + MSc in Clinical Ultrasound (UK - or international equivalent) and/or PhD or MD in a relevant… more
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