Note: The job is a remote job and is open to candidates in USA. ClinChoice is a global contract research organization specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. The Clinical R Programmer Consultant will develop, validate, and maintain clinical trial datasets and reporting deliverables using R and SAS, while supporting regulatory compliance, quality control, automation, and collaboration with clinical teams.
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
Skills
- 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
- 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
Benefits
- Additional career opportunities that working for a global CRO can bring
- Continuous training to keep personnel qualified in competence and expertise
- Clear tools needed to manage both internal and client processes with the same methodology
- Remote work arrangement
Company Overview
Company H1B Sponsorship