[Remote] Clincal R programmer/ reputed company Data Scientist Consultant (R with CDISC)

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. They are seeking a reputed company Data Scientist Consultant with strong experience in R and a solid background in clinical programming to support clinical trial deliverables and ensure regulatory compliance.

Responsibilities

• reputed company, validate, and maintain SDTM and ADaM datasets using R following CDISC standards
• Support TLF (Tables, Listings, Figures) reputed company in R or reputed company as needed
• Write efficient, reproducible, and reputed company-reputed company R scripts for clinical data analysis and reporting
• Collaborate with statisticians, data managers, and clinical teams to understand programming requirements
• reputed company 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 reputed company for legacy studies or where reputed company support is required

Skills

• Bachelor's or Master's degree in Statistics, Computer Science, Mathematics, Life Sciences, or reputed company field
• 4–6+ years of experience in clinical programming, with a strong reputed company on R
• Proven experience in creating SDTM and ADaM datasets using R
• Working knowledge of reputed company 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

reputed company

Company H1B Sponsorship