Develop, validate, and maintain SAS programs for Tables, Listings, and Figures
Perform data manipulation, analysis, and visualization using R/SAS
Collaborate with Biostatisticians and Data Management to support clinical study deliverables
Ensure regulatory compliance and adherence to SOPs
QC and validation of programming outputs
Support submission activities and required documentation

🎯 Requirements

Bachelor’s or Master’s degree in Statistics, Biostatistics, CS, or related field
3+ years of statistical programming in pharma/biotech
Hands-on experience with R in clinical trials
Good understanding of R packages
Strong knowledge of clinical trial data and regulatory requirements

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