Clinical R Programmer Consultant

📋 Description

• Design, develop, and maintain clinical programming deliverables for trials and regulatory needs.
• Develop, validate, and maintain SDTM and ADaM datasets using R per CDISC standards.
• Create efficient, reproducible R scripts for data analysis and automation.
• Support TLFs (tables, listings, figures) with R and SAS when needed.
• Collaborate with statisticians, data managers, and cross-functional teams.
• Perform QC, investigate data discrepancies, ensure regulatory-compliant outputs.

🎯 Requirements

• Bachelor’s or Master’s in Statistics, CS, Math, Life Sciences, or related field.
• 2+ years of clinical programming experience with strong R.
• Experience creating SDTM and ADaM datasets using R.
• Working knowledge of SAS in a clinical research environment.
• Strong understanding of CDISC SDTM/ADaM standards.
• Experience supporting trials, submissions, and QC processes.

🎁 Benefits

• Opportunity to work with a dedicated client within a global organization.
• Remote work flexibility.
• Exposure to modern R-based clinical programming practices.
• Impactful clinical development programs contribution.
• Collaborative environment with clinical, statistical, and data teams.
• Professional development and continuous learning opportunities.