Develop, validate, and maintain SDTM and ADaM datasets using R following CDISC standards
Support Tables, Listings, and Figures (TLF) generation in R or SAS as needed
Write efficient, reproducible R scripts for clinical data analysis and reporting
Collaborate with statisticians, data managers, and clinical teams to understand programming
Perform QC checks, reconcile data issues, and ensure regulatory deliverables meet FDA/EMA
Contribute to programming workflows, documentation, and version control best practices

🎯 Requirements

Bachelor’s or Master’s degree in Statistics, Computer Science, Mathematics, Life Sciences, or
2-3+ years of experience in clinical programming, with strong focus on R
Proven experience creating SDTM and ADaM datasets using R
Working knowledge of SAS programming
Solid understanding of CDISC standards (SDTM, ADaM)
Experience with clinical trial data, regulatory submissions, and QC processes

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