Principal Computational Statistician

Role: Statistical analyst supporting clinical studies at Lilly, focusing on data analysis, report writing, and regulatory communication. Responsibilities: collaborate on statistical analysis plans, select and justify analytical methods, ensure data quality, and communicate results for regulatory submissions. Maintain proficiency in SAS/R, stay current on system and disease knowledge, and adhere to GxP and regulatory compliance. Qualifications: Master’s in Statistics, Biostatistics, or related field; 2+ years of programming and analysis experience. Preferred skills include proficiency in SAS, R, and visualization tools, strong interpersonal skills, and problem-solving ability. High-Value: clinical trials, biopharma, statistical analysis, data quality, regulatory communication, applicable to various therapeutic areas. Work setup: full-time, with compensation depending on experience and location, with comprehensive benefits.