Develop, validate, and maintain SDTM and ADaM datasets using R per CDISC standards.
Support TLF (Tables, Listings, Figures) generation in R or SAS as needed.
Write efficient, reproducible R scripts for clinical data analysis and reporting.
Collaborate with biostatistics and clinical data teams to define programming requirements.
Perform QC checks, reconcile data issues, and ensure regulatory deliverables (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 related field.
4–6+ years of experience in clinical programming, with a 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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