- Cytel (Boston, MA)
- …& R-Shiny. + At least 5 years of R/ SAS programming experience with clinical trial data . + General knowledge of regulatory requirements and drug development ... programmer will also be required to utilize the SAS software system; they should be proficient in ...support electronic regulatory submissions; providing systems and support for clinical data management staff, clinical … more
- Cytel (Boston, MA)
- …Performing data manipulation, analysis and reporting of clinical trial data , both safety and efficacy (ISS/ISE), utilizing SAS programming + Production ... this new program. **Position Overview:** As a Senior Statistical Programmer , you will leverage your advanced SAS ...8 years of SAS programming working with clinical trial data in the Pharmaceutical &… more
- Cytel (Cambridge, MA)
- …Clinical Development, and other functional representatives to develop, maintain and document clinical data standards. This role also acts as a statistical ... + Provides technical and/or operational guidance in the application of industry clinical data standards within the statistical programming data … more
- Sanofi Group (Cambridge, MA)
- …**Main Responsibilities:** + Provide high quality input into the design of the clinical study (including protocol development), the setup and conduct of the study to ... make sure data are adequately captured and collected to answer the...quality control plan. + Perform and/or coordinate with study programmer the production of statistical analyses. Review and examine… more
- Sanofi Group (Cambridge, MA)
- …critical in helping our teams accelerate progress. Join our B&P Neurology team as a Data Analyst and you'll lead one or several late phase studies, or lead an ... Provide high quality input into the design of the clinical study, the setup and conduct of the study...the statistical analysis plan: perform and/or coordinate with study programmer the production of statistical analyses + Prepare statistical… more