Clinical R programmer Consultant

📋 Description

• Develop, validate, and maintain SDTM and ADaM datasets using R following CDISC standards.
• Support Tables, Listings, Figures generation in R or SAS as needed.
• Write efficient, reproducible, and well-structured R scripts for clinical data analysis and
• Collaborate with statisticians, data managers, and clinical teams to understand programming
• Perform QC checks, reconcile data issues, and ensure deliverables meet regulatory expectations
• Contribute to programming workflows, documentation, and version control best practices.

🎯 Requirements

• Bachelor’s or Master’s degree in Statistics, Computer Science, Mathematics, Life Sciences, or
• 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.

🎁 Benefits

• Opportunity to work directly for a sponsor while enjoying CRO career opportunities.
• Global team with 28+ years of experience and 4,000+ professionals.