Clinical R programmer Consultant
About The Position
ClinChoice is seeking a Clinical R Programmer Consultant to join one of our clients. This role offers the unique opportunity to work directly for a single sponsor while benefiting from the security and career advancement possibilities of a global CRO. The ideal candidate will possess strong R programming skills and a robust background in clinical programming, with hands-on experience in developing SDTM and ADAM datasets using R. Familiarity with SAS is also required. This position is crucial for supporting clinical trial deliverables, ensuring adherence to regulatory compliance, and fostering collaboration between biostatistics and clinical data teams.
Requirements
- Bachelor’s or Master’s degree in Statistics, Computer Science, Mathematics, Life Sciences, or related field.
- 2-3+ 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.
Nice To Haves
- Experience with R packages such as tidyverse, haven, pharmaverse (e.g., admiral, tidyCDISC), or other clinical programming toolkits.
- Understanding of R Markdown, Shiny apps, or reproducible reporting tools.
- Exposure to GxP validation, version control (Git), and automated workflows.
- Experience working in a CRO or pharmaceutical environment.
Responsibilities
- 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.
Benefits
- Security and additional career opportunities that working for a global CRO can bring.
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What This Job Offers
Job Type
Full-time
Career Level
Senior
