|仕事内容||■Act as a Trial Statistician (TSTAT) for multiple (more than three) clinical trials as Project Statistician (PSTAT) for early projects, backup projects, or projects with established BI experience or act as a PSTAT-Medical Affairs for projects with established BI experience.
■Act as a co-PSTAT on complex, major drug projects by planning and supervising specific areas of a drug submission (e.g. for the integrated summary of safety) or for an across-study analysis project (e.g. for publication) or by taking over other PSTAT tasks under supervision.
■Promote efficient, innovative and robust drug development processes, with emphasis on the analysis and reporting of clinical data by participating in international working groups or by acting as a team leader for complex analysis projects.