Clinical R Programmer Consultant

Clinical R Programmer Consultant for ClinChoice developing datasets and supporting clinical trial deliverables while ensuring regulatory compliance.

Posted 5/8/2026full-timeRemote • 🇺🇸 United StatesMid-LevelSeniorWebsite

Key responsibilities & impact

Develop, validate, and maintain SDTM and ADaM datasets using R following CDISC standards.
Support TLF (Tables, Listings, Figures) generation in R or SAS as needed.
Write efficient, reproducible, and well-structured R scripts for clinical data analysis and reporting.
Collaborate with statisticians, data managers, and clinical teams to understand programming requirements.
Perform QC checks, reconcile data issues, and ensure deliverables meet regulatory expectations (e.g., FDA, EMA).
Contribute to programming workflows, documentation, and version control best practices.
Support automation initiatives and R-based pipeline development.
Utilize SAS for legacy studies or where SAS support is required.

What you’ll need

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 in 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.
Strong analytical, problem-solving, and documentation skills.

Comp & perks

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Hard Skills & Tools

RSASSDTMADaMclinical data analysisTLF generationdata reconciliationQC checksprogramming workflowsautomation

Soft Skills

analytical skillsproblem-solving skillsdocumentation skillscollaborationcommunication