
Clinical R Data Scientist Consultant
Posted 1 day ago

Posted 1 day ago
This is a fully remote position, open to applicants in United States.
• Design, validate, and sustain SDTM and ADaM datasets utilizing R in accordance with CDISC standards.
• Assist in the generation of TLF (Tables, Listings, Figures) in R or SAS as required.
• Create efficient, reproducible, and well-organized R scripts for clinical data analysis and reporting.
• Collaborate with statisticians, data managers, and clinical teams to comprehend programming needs.
• Conduct QC checks, resolve data discrepancies, and ensure deliverables comply with regulatory standards, including FDA and EMA guidelines.
• Contribute to programming workflows, documentation, and best practices for version control.
• Aid in automation efforts and the development of R-based pipelines.
• Employ SAS for legacy studies or in situations where SAS support is necessary.
• Bachelor’s or Master’s degree in Statistics, Computer Science, Mathematics, Life Sciences, or a related field.
• 2-3+ years of experience in clinical programming, with a strong emphasis on R.
• Demonstrated experience in creating SDTM and ADaM datasets using R.
• Proficient understanding of SAS programming.
• Comprehensive knowledge of CDISC standards (SDTM, ADaM).
• Experience with clinical trial data, regulatory submissions, and QC processes.
• Strong analytical, problem-solving, and documentation abilities.
• Familiarity with R packages such as tidyverse, haven, pharmaverse (e.g., admiral, tidyCDISC), or other clinical programming tools.
• Understanding of R Markdown, Shiny apps, or tools for reproducible reporting.
• Exposure to GxP validation, version control (Git), and automated workflows.
• Experience in a CRO or pharmaceutical setting.
• Ongoing training and career development opportunities.
• Supportive management and training.
• Commitment to equal opportunity, diversity, and inclusivity.
• Opportunity to work directly for a single sponsor, with the security and additional career prospects provided by a global CRO.
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