- 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
- Takeda Pharmaceuticals (Lexington, MA)
- …company to inspire you and empower you to shine? Join us as an Associate Director , Vendor Management ( Clinical Supplies) based in Lexington, MA ... will be a necessary contributor to our inspiring, bold mission. **GOALS:** + The Associate Director , Vendor Management ( Clinical Supplies) is responsible for… 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 (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
- 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
- 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