Sr. Computational Statistician

Role: Biostatistician supporting clinical trial analysis in the biopharma context, focusing on data analysis, statistical methods, and regulatory communication. Responsibilities: collaborate on analysis plans, conduct statistical analysis using SAS/R, ensure data quality, and communicate results for regulatory submissions and publications. Requirements: Master’s in Statistics, Biostatistics, or MSPH; proficiency in SAS, R, or similar tools; strong understanding of statistics and data analysis; effective communication and teamwork skills. HighValue: clinical trials, statistical analysis, regulatory support, biopharma data systems. WorkSetup: not specified; likely office-based or hybrid, with emphasis on technical proficiency.