
Clinical R Programmer, SDTM/ADaM, Contract role
ClinChoice
contract
Posted on:
Location Type: Remote
Location: Remote • 🇺🇸 United States
Visit company websiteJob Level
JuniorMid-Level
About the role
- 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.
Requirements
- Bachelor’s or Master’s degree in Statistics, Computer Science, Mathematics, Life Sciences, or related field.
- 2–6+ 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.
Benefits
- ClinChoice offers flexible work arrangements
- Professional development opportunities
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
RSASSDTMADaMclinical data analysisTLF generationdata reconciliationQC checksprogramming workflowsautomation
Soft skills
analytical skillsproblem-solvingdocumentation skillscollaborationcommunication