- 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 ... of clinical deviation management and Serious Breach process across Clinical Program Quality. + Acts as Subject Matter Expert (SME) for clinical… more
- Rhythm Pharmaceuticals (Boston, MA)
- …overcome barriers, together. Opportunity Overview Rhythm Pharmaceuticals is seeking an Associate Director , Non- Clinical Research with demonstrable experience ... company strategy. This role will report into the Sr. Director , Non- Clinical Development. Responsibilities and Duties +...for clinical studies + Strong understanding of non- clinical safety toxicology program with experience in… more
- Takeda Pharmaceuticals (Lexington, MA)
- …my employment application is true to the best of my knowledge. **Job Description** ** Associate Director , Clinical Research, Value & Evidence Generation, US ... study design, and good clinical practice. + Strong clinical research and program management experienced in leading cross-functional clinical programs… more
- 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 ... + Experience must include successful development and implementation of a clinical or pharmacovigilance audit program , hosting/leading regulatory inspections,… more
- Takeda Pharmaceuticals (Lexington, MA)
- …is true to the best of my knowledge. **Job Description** **About the Role:** The Associate Director of Device Clinical Development (DCD) in the Drug Product ... 5 days per month) is strongly preferred + Advanced program management skills + Strong background in clinical... program management skills + Strong background in clinical research methodology + Exceptional stakeholder management and conflict… more
- Bristol Myers Squibb (Boston, MA)
- …biology, mechanism of action, and predictive biomarkers in our late-stage clinical oncology portfolio. Ideal candidates will possess a strong scientific background, ... communication skills, and experience working in a matrixed industrial environment. The Clinical Biomarker Asset Lead role will be responsible for development and… more
- Bristol Myers Squibb (Cambridge, MA)
- …of the Global Research organization in BMS and leads late stage clinical , pharmacological and translational research and development activities for the pipeline and ... immunology, cardiovascular and neuroscience. This group integrates laboratory science, clinical trial/biomarkers and asset development as well as disease research… more
- Takeda Pharmaceuticals (Boston, MA)
- …**Job Description** **OBJECTIVES:** + Provides oversight from a clinical research and pharmacovigilance perspective of regulated post-authorization activities ... units and the affiliate and enables them to deliver their clinical research and pharmacovigilance-related regulated activities with high compliance and agility.… more
- Dana-Farber Cancer Institute (Brookline, MA)
- …Cancer Center, the Director will also work closely with the DF/HCC Associate Director of Clinical Trials and DF/HCC Medical Director ... is to develop, maintain, implement and continuously improve a program that supports the highest standards of data quality...that supports the highest standards of data quality in clinical research. The Director is responsible for… more
- Dana-Farber Cancer Institute (Boston, MA)
- …hospitals. The Statistician in this role will have the title Associate Director of the Breast Oncology Statistical Program and is expected to work ... participant in the articulation of the collaborative vision, working with program leaders and clinical research directors on scientific program direction and… more
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