Clinical R Programmer – SDTM/ADaM (Remote – US, Contract)
Location: United States (Remote)
Employment Type: Contract / Full-Time
Experience Required: 2–6+ Years in Clinical Programming
Educational Qualification: Bachelor’s or Master’s in Statistics, Computer Science, Mathematics, Life Sciences, or related field
Job Overview
ClinChoice, a global full-service CRO, is seeking a Clinical R Programmer with hands-on experience in SDTM and ADaM dataset creation using R, complemented by working knowledge of SAS. This role focuses on supporting clinical trial deliverables, ensuring regulatory compliance, and collaborating with biostatistics, clinical data, and programming teams for high-quality study outputs.
The ideal candidate is skilled in R programming for clinical data management, TLF generation, reproducible reporting, and automation workflows, while understanding CDISC standards and regulatory expectations.
Key Responsibilities
Clinical Programming & Data Management
Develop, validate, and maintain SDTM and ADaM datasets using R in compliance with CDISC standards.
Support Tables, Listings, and Figures (TLFs) generation using R or SAS as required.
Write efficient, reproducible, and well-structured R scripts for clinical data analysis and reporting.
Perform quality control checks, reconcile data issues, and ensure outputs meet regulatory standards (FDA, EMA).
Collaboration & Workflow Support
Collaborate with statisticians, data managers, and clinical teams to understand programming requirements.
Contribute to programming workflows, documentation, and version control best practices.
Support automation initiatives, pipeline development, and reproducible reporting tools.
Utilize SAS for legacy studies or as necessary for specific programming deliverables.
Required Qualifications
Bachelor’s or Master’s in Statistics, Computer Science, Mathematics, Life Sciences, or related field.
2–6+ years of clinical programming experience with strong R expertise.
Proven experience developing SDTM and ADaM datasets using R.
Working knowledge of SAS programming.
Solid understanding of CDISC standards (SDTM, ADaM).
Familiarity with clinical trial data, regulatory submissions, and QC processes.
Strong analytical, problem-solving, and documentation skills.
Preferred Qualifications
Experience with R packages such as tidyverse, haven, pharmaverse (e.g., admiral, tidyCDISC).
Knowledge of R Markdown, Shiny apps, or other reproducible reporting tools.
Exposure to GxP validation, version control (Git), and automated workflows.
Previous experience working in a CRO or pharmaceutical environment.
Why Join ClinChoice?
Work directly for a single sponsor while benefiting from the resources of a global CRO.
Support high-impact clinical trials with advanced R programming and clinical data solutions.
Join a diverse and inclusive culture that prioritizes training, professional growth, and collaboration.
Contribute to automation, reproducibility, and innovation in clinical programming workflows.
Apply now to join ClinChoice as a Clinical R Programmer – SDTM/ADaM and play a key role in regulatory-compliant clinical trial programming for global studies.
Explore more clinical data science, statistical programming, and R programming opportunities at thepharmadaily.com.
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