A company is looking for a Principal R Programmer to analyze and report clinical trial data remotely.
Key Responsibilities
Design, develop, and validate R programs for statistical analysis and reporting of clinical trial data
Collaborate with biostatisticians to create analysis plans and apply statistical methods
Perform quality control checks and assist in preparing statistical reports and regulatory submissions
Required Qualifications
Bachelor's or Master's degree in Statistics, Mathematics, Computer Science, or a related field
Significant experience in statistical programming within the clinical research or pharmaceutical industry
Strong proficiency in R programming and understanding of statistical concepts
Knowledge of CDISC standards (SEND, SDTM, and ADaM) is required
Experience with advanced R programming tools such as tidyverse, ggplot2, and Shiny
Programmer • Minneapolis, Minnesota, United States