- Takeda (Boston, MA)
- …to the best of my knowledge. Job Description About the role: The Associate Director , Clinical & Quality Process Compliance is responsible for ensuring the quality of ... are considered. Enable a compliant quality system in safety and clinical trial delivery systems via CPMQ continual improvements projects. Actively participate and… more
- Vertex Pharmaceuticals (Boston, MA)
- …clinical trials , observational studies, or real world data (RWD) investigations .* Leads biostatistics projects or major components of a project including work ... **Job Description The Associate Director , Biostatistics** will perform sophisticated scientific statistical analyses in support of the company's Global Medicines… more
- Merck (Boston, MA)
- …Clinical Investigations , Clinical Judgment, Clinical Medicine, Clinical Research, Clinical Trial Designs, Clinical Trial Planning, Clinical Trials , ... dedicated colleagues while developing and expanding your career. The Clinical Director (Principal Scientist) has primary responsibility for the planning and… more
- Sanofi Group (Cambridge, MA)
- …as needed. + He/she ensures appropriate review and consistency of the data and investigations of safety cases with the Clinical Trial Team (Monitoring Teams) or ... **Job Title:** Development Scientific Director **Location:** Morristown, NJ Cambridge, MA **About the...study documents and activities from clinical development plans and trial set-up to clinical study report in compliance with… more
- Takeda Pharmaceuticals (Boston, MA)
- …best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical & Quality Process Compliance is responsible for ensuring the quality ... considered. + Enable a compliant quality system in safety and clinical trial delivery systems via CPMQ continual improvements projects. Actively participate and… more
- Bristol Myers Squibb (Devens, MA)
- …in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director Stability is responsible for stability product strategy and oversight of ... and approval of stability reports and regulatory filings. The Associate Director is responsible for leading high-performance technical team, developing team and… more
- Bristol Myers Squibb (Devens, MA)
- …. **Position Summary** Bristol-Myers Squibb is seeking an Associate Director , Principal Product Quality Leader (PQL), in Global Product Quality ... process/manufacturing, control strategy, analytical methods, specifications, reference standards, stability, investigations , change control, product complaints, and regulatory submissions. The… more
- Bristol Myers Squibb (Devens, MA)
- …procedure. + Provide Subject Matter expertise for root cause evaluations, investigations , deviations, change management, and corrective actions. + Perform Power ... significant program delays and financial impact. + Position is supervised by Director , Utilities & Sustainability. Daily direction and alignment is not required.… more
