- Takeda Pharmaceuticals (Boston, MA)
- …true to the best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical and Safety Quality Compliance is responsible for ... process in partnership with functional compliance teams for regulations impacting Clinical , Safety and Clinical Pharmacovigilance Medical Quality (CPMQ)… more
- Takeda Pharmaceuticals (Boston, MA)
- …is true to the best of my knowledge. **Job Description** **About the role:** Associate Director , Clinical Program Quality Investigations is responsible for ... supports Takeda's mission by maintaining high standards of quality and compliance in clinical trials. **How will you contribute:** + Drive the implementation of … more
- Bristol Myers Squibb (Cambridge, MA)
- …Operations and Procurement. + Determines appropriate assays and vendors for clinical biomarkers, and manages outsourcing of biomarker assay development ... of the Global Research organization in BMS and leads late stage clinical , pharmacological and translational research and development activities for the pipeline and… more
- CenterWell (Boston, MA)
- …expansion, vendor allocation, outsourcing , and automation. Additionally, the Associate Director collaborates with Real-Time Management, Scheduling, and ... caring community and help us put health first** The Associate Director of WFM Capacity Planning is...chronic and complex illnesses, as well as offer personalized clinical and educational services to improve health outcomes and… more
- Takeda Pharmaceuticals (Boston, MA)
- …improvement + Lead CPMQ continuous improvement initiatives to enable optimization of clinical and safety quality compliance activities. + Provide expert advice and ... metrics for CPMQ activities eg audit, inspection, QE, CAPA. + Organise Clinical and Pharmacovigilance Quality council meetings and proactively manage the agenda and… more
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