Job Summary
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
Comments