Description
The role contributes to statistical programming for global clinical trials by developing analysis data sets, program requirements and specifications, SAS programs for ADS, tables, listings and figures, program validations, documentation, and TFLs. The position collaborates with international statisticians, programmers, and data managers and requires a university and master's degree in a relevant field, clinical-trials or biostatistics experience, SAS knowledge, strong analytical and communication skills, and proficiency in English and Microsoft Office.
