Applying advanced statistical methods to project work.
Ensuring scientific integrity in the application of statistical methodology to clinical trials.
Participate as senior statistician on major projects, including developing/reviewing protocols, preparing analysis plans, overseeing the conduct of analyses, and preparing integrated clinical and statistical reports.
? Perform statistical team lead role on single studies.
? Develop statistical methods sections of protocols and review case report forms (CRFs).
? Prepare analysis plans and write specifications for analysis files, ｔａｂｌｅs, and figures.
? Communicate with clients regarding study protocol or statistical analysis issues as they arise.
? Communicate with study team members regarding study ｅｘｅｃution as it relates to timelines, data quality, and interpretation of results.
? Interpret analyses and write statistical sections of study reports.
Conduct independent research and teaches courses in statistical methodology.

? Bachelor’s Degree Biostatistics with 7+ years experience Req Or ｍａｓｔｅｒ’s Degree Biostatistics with 5+ years experience Or Ph.D. Biostatistics with 2+ years experience
? Familiarity with most complex statistical methods that apply to Phase I-IV clinical trials.
? In-depth knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guiｄｅｌines.
? Strong working knowledge of SAS.
? Excellent written and oral communication skills with good interpersonal skills.
? Excellent problem solving skills.