- 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 ... process in partnership with functional compliance teams for regulations impacting Clinical , Safety and Clinical Pharmacovigilance Medical Quality… 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)
- …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 ... activities across clinical , regulatory, quality, and engineering functions + Perform safety reviews on device and combination products from clinical trials… 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 ... that supports the highest standards of data quality in clinical research. The Director is responsible for...across the DF/HCC consortium, support for the DF/HCC Data Safety Monitoring Board/Committee as well as maintenance of the… more
- Merck (Boston, MA)
- …to manage clinical development projects; and assist the Executive Director and/or Associate Vice President in ensuring that appropriate Corporate ... medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will...clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications,… more
- Sanofi Group (Cambridge, MA)
- **Job Title:** Associate Director , Global Regulatory Affairs - Global Labeling Strategy **Location** : Morristown, NJ or Cambridge, MA (Hybrid) **About the Job** ... Your skills could be critical in helping our teams accelerate progress. The Associate Director , Global Regulatory Affairs - Global Labeling Strategy is… more
- Sumitomo Pharma (Boston, MA)
- …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate Medical Director .** The Associate Medical Director ... risk/benefit assessment for assigned investigational and marketed products. + Conduct safety surveillance over product life cycle, reviewing clinical trial… more
- Takeda Pharmaceuticals (Boston, MA)
- …you and empower you to shine? Join us as a PV Risk Management Scientist/ Associate Director . At Takeda, we are transforming the pharmaceutical industry through ... strive for excellence in everything we do. As an Associate Director / PV Risk Management Scientist, being...benefit-risk activities (eg patient preference studies) + Collaborate with Safety Leads, Clinical Leads, PV scientists and… more
- Takeda Pharmaceuticals (Boston, MA)
- …possible in order to bring life-changing therapies to patients worldwide. The Associate Director , Global Regulatory Affairs Advertising and Promotion (GRA A&P) ... to prescription medicine promotion. **How you will contribute:** + As our Associate Director , Global Regulatory Affairs Advertising and Promotion lead you… more
- Bristol Myers Squibb (Devens, MA)
- …no better place than here at BMS with our Cell Therapy team. The ** Associate Director ,** **Process Implementation Lead l** eads the transition of hybrid ... sharing, and best practice adoption. + Model BMS values, promoting safety , inclusion, innovation, and operational excellence. **Knowledge & Skills:** + Proven… more
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