Job Title: Clinical R Programmer – SDTM/ADaM (Contract, Remote)
Location: United States (Remote)
Employment Type: Contract
Posted: Recently
About the Role:
ClinChoice, a global full-service CRO, is seeking a Clinical R Programmer Consultant with strong R programming expertise and experience in SDTM and ADaM dataset development. This role offers the unique opportunity to work directly with a single sponsor while leveraging the professional support, career growth, and global exposure provided by a leading CRO.
As a Clinical R Programmer, you will support clinical trial deliverables, ensure regulatory compliance, and collaborate with biostatistics and clinical data teams to generate high-quality datasets and analyses.
Key Responsibilities:
Develop, validate, and maintain SDTM and ADaM datasets using R according to CDISC standards.
Support Tables, Listings, and Figures (TLF) generation in R or SAS as required.
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 discrepancies, and ensure deliverables meet regulatory expectations (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 necessary.
Required Qualifications:
Bachelor’s or Master’s degree in Statistics, Computer Science, Mathematics, Life Sciences, or related field.
2–6+ years of clinical programming experience, with strong R programming expertise.
Hands-on 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.
Strong analytical, problem-solving, and documentation skills.
Preferred Qualifications:
Experience with R packages such as tidyverse, haven, or pharmaverse (admiral, tidyCDISC).
Knowledge of R Markdown, Shiny apps, or reproducible reporting tools.
Familiarity with GxP validation, version control (Git), and automated workflows.
Prior experience in a CRO or pharmaceutical environment.
Why ClinChoice:
ClinChoice is a global CRO with over 28 years of experience delivering high-quality clinical development solutions across pharmaceutical, biotechnology, medical device, and consumer health industries. With more than 4,000 professionals across 20+ countries, we foster a culture of training, professional development, and excellence while ensuring employees are fully supported in their careers.
Equal Opportunity Statement:
ClinChoice is an equal opportunity employer, committed to diversity, inclusion, and celebrating employees from all backgrounds, genders, races, beliefs, and ethnicities.
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