Clinical R Programmer Consultant
C
ClinChoicePharmaceutical
Location: United StatesContractSenior
Salary not disclosed
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Job Details
- Experience
- 4–6+ years of experience
- Required Skills
- Analytical SkillsProblem-solving skillsR
Requirements
- Bachelor’s or Master’s degree in Statistics, Computer Science, Mathematics, Life Sciences, or related field.
- 4–6+ 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.
- 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.
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