Develop, validate, and maintain SDTM and ADaM datasets using R per CDISC standards.
Support 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 define programming needs.
Perform QC checks, resolve data issues, and ensure regulatory deliverables.
Contribute to programming workflows, docs, and version control best practices.

🎯 Requirements

Bachelor's or Master’s in Statistics, CS, Math, Life Sciences, or related field.
4–6+ years of experience in clinical programming with focus on R.
Proven experience creating SDTM and ADaM datasets using R.
Working knowledge of SAS programming.
CDISC standards (SDTM, ADaM) understanding and strong analytical skills.
Experience with clinical trial data, regulatory submissions, and QC processes.

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