- Pfizer (Cambridge, MA)
- …Development-focused technological innovation, and work with Pfizer Medical Strategy and Scientific Affairs colleagues on external communications on these topics. ... Advanced degree (either Master's or PhD) degree in relevant scientific / medical subject. + If Masters: 15+ years...with expert knowledge in clinical trial conduct, clinical, monitoring& regulatory operations. + If PhD: 10+ years in clinical… more
- Takeda Pharmaceuticals (Boston, MA)
- …best of my knowledge. **Job Description** **About the role:** Associate Director , Clinical Program Quality Investigations is responsible for ensuring the compliance ... deviation management, and Serious Breaches investigation and reporting to regulatory agencies. + Act as strategic partner to Clinical...**What you bring to Takeda:** + BSc in a scientific or allied health/medical field (or equivalent degree). +… more
- J&J Family of Companies (Cambridge, MA)
- …and external human data resources. + Partner with Clinical Development, Global Regulatory Affairs , Data Science, Patient Reported Outcomes, Statistics and other ... while championing patients every step of the way. We are searching for a ** Director , Computational Multiomics, Neuroscience,** to be located at one of our offices in… more
- Takeda Pharmaceuticals (Boston, MA)
- …processes and training and ensure alignment with global processes and regulatory requirements and expectations. + Drive the implementation and change management ... enable execution of CPMQ activities, ensuring alignment with global processes and regulatory requirements. + Create and deliver training solutions to support the… more
- Takeda Pharmaceuticals (Boston, MA)
- …limited to PSPV sub-functions, Documentation & Learning Excellence (DLE), Global Regulatory Affairs (GRA), Global Development Organization (GDO), Clinical ... employee onboarding and training activities. + Monitors, interprets, and communicate regulatory requirements and ensure global standards, SOPs, and all associated… more
- Merck (Boston, MA)
- …Project Reviews, Prostate Cancer, Regulatory Affairs Compliance, Regulatory Compliance, Regulatory Reporting, Scientific Publications, Strategic ... + Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …TA. + Acts as a senior company representative interacting with external scientific leaders, patient advocacy groups and/or regulatory authorities. + Establishes ... scientific leaders, policy makers, patient advocacy groups and/or regulatory authorities. + Establishes and/or enhances partnerships with key academic… more
- Sanofi Group (Cambridge, MA)
- …HEOR Biostatistician **Location** : Cambridge, MA Morristown, NJ **Level:** Sr. Manager/Associate Director equivalent **About the Job** Are you ready to shape the ... aligns with several stakeholders including Market Access and Pricing, Medical Affairs , Clinical Outcome Assessment teams, Biostatistics, etc. We are an innovative… more
- Curia (Hopkinton, MA)
- …to products, processes, and services to achieve a consistent approach to Quality Assurance and Regulatory Affairs + Acts as a key point of contact with customers ... leadership and drives Quality decisions at the site and also supports regional Director of Quality for global Quality initiatives + Provides hands on leadership and… more
- Fujifilm (Boston, MA)
- …expense tracking and reporting (Salesforce.com) + Where appropriate, collaborate with the Medical Affairs Team. + Follow up to define pathway and respond to customer ... all capital equipment i30 placements as directed by the Director of Sales and Marketing. + The territory is...US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all… more