Clincal R programmer/ Principal Data Scientist Consultant (R with CDISC)

📋 Description

• Develop, validate, and maintain SDTM/ADaM datasets in R per CDISC.
• Support TLF generation in R or SAS as needed.
• Write efficient, reproducible R scripts for clinical data analysis and reporting.
• Collaborate with statisticians, data managers, and clinical teams to define programming needs.
• QC checks, resolve data issues, and ensure regulatory-ready deliverables.
• Automate pipelines and support version control best practices.

🎯 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 strong focus on R.
• Proven experience creating SDTM and ADaM datasets using R.
• Working knowledge of SAS.
• Solid understanding of CDISC standards (SDTM, ADaM).
• Experience with clinical trial data, regulatory submissions, and QC processes.

🎁 Benefits

• Global CRO with extensive career opportunities.
• 4,000+ professionals across 20+ countries.
• Equal opportunity employer with commitment to diversity.