- Takeda Pharmaceuticals (Lexington, MA)
- …to the best of my knowledge. **Job Description** **About the Role:** The Associate Director of Device Clinical Development (DCD) in the Drug Product and Device ... Development (DPDD) group provides strategic clinical leadership for global device and combination product development programs. This pivotal role involves… more
- Pfizer (Cambridge, MA)
- …other statisticians, study managers, alliance partner colleagues - for assigned studies and regulatory submissions. + Provide input to the Statistics Group Lead ... Pfizer Research and Development. The candidate's accountabilities include overseeing clinical design, trial conduct, data management, result interpretation, and...(Senior Director or Executive Director ) to plan support for assigned studies … more
- Dana-Farber Cancer Institute (Brookline, MA)
- …continuously improve a program that supports the highest standards of data quality in clinical research. The Director is responsible for the oversight of ... data and oversight of DF/HCC policies and procedures. Reporting to the VP Clinical Research Management Dana-Farber/Harvard Cancer Center, the Director will also… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …these activities, and is accountable for the successful design and interpretation of clinical studies . Presents study conclusions to Management and determine ... **Synopsis / Protocol Development, Study Execution, & Study Interpretation** + Drives clinical science activities.../ approval of synopses, protocols and the conduct of clinical studies . Serves as an advisor to… more
- Bausch + Lomb (Boston, MA)
- …**Position Summary** **:** Is responsible for the implementation and oversight of clinical study operations by organizing and coordinating with other relevant ... parties the planning, implementation, management, execution and completion of clinical studies according to applicable regulations and guidance, ICH and GCP, and… more
- AbbVie (Boston, MA)
- …and AbbVie study staff. + Has responsibility for oversight of clinical studies , monitoring overall study integrity, and review, interpretation, ... interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses, and other… more
- Pfizer (Cambridge, MA)
- …The successful candidate will collaborate closely with cross-functional project and study teams, offering statistical expertise in designing clinical trials, ... input and leadership to cross-functional activities - collaborate with other statisticians, study managers, programmers - for assigned studies and regulatory… more
- Sanofi Group (Cambridge, MA)
- …of what you thought was possible. Ready to get started? **Main Responsibilities:** ** Clinical Study Leadership** + Provide scientific expertise for study ... , Safety Officer and Pharmacovigilance, Translational Medicine, Regulatory Affairs, Biostatistics, Clinical Study Units, Medical Affairs, and CROs to optimize… 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
- Takeda Pharmaceuticals (Boston, MA)
- …utilization of high-dimensional datasets, including multi-omics data from translational and clinical studies , to support the IBD strategy. This includes ... develop cutting-edge analytical strategies, and support data-driven decision-making across the clinical development continuum. + As Director , you will lead… more
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