- Takeda Pharmaceuticals (Boston, MA)
- …best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical and Safety Quality Compliance is responsible for ensuring the quality ... and monitoring processes, and ensuring compliance with corporate and regulatory standards. By maintaining high-quality standards, this role supports Takeda's… more
- Takeda Pharmaceuticals (Boston, MA)
- …inspire you and empower you to shine? Join us as a Executive Medical Director , Oncology Clinical Sciences in our Cambridge office. At Takeda, we are transforming the ... development plan that is competitive and consistent with the latest regulatory requirements, proactive identification of challenges, and development of contingency… more
- Takeda Pharmaceuticals (Boston, MA)
- …communicate safety issues with other functional areas such as Clinical Development, Regulatory Affairs , Quality Assurance, Medical Affairs , Marketing, ... data from various sources including non-clinical, clinical, post-marketing and scientific literature. + Conduct signal detection, monitoring, evaluation, interpretation,… more
- 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
- 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)
- …, Clinical Outcomes Assessment (COA) and Health Value Translation (HVT) + Public Affairs , Communications + Regulatory Affairs , Compliance and Legal External: ... **Job Title:** Director , HEVA Business Partner - Multiple Myeloma **Location:**...The incumbent will interface with Market Access, Clinical, Medical Affairs , and Commercial teams including Global and US. The… more