Clinical R Programmer Consultant

This is a fully remote position, open to applicants in United States.

📋 Description

• Develop, validate, and maintain SDTM and ADaM datasets using R in accordance with CDISC standards.

• Assist in the generation of TLF (Tables, Listings, Figures) using R or SAS as required.

• Create efficient, reproducible, and well-structured 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 that deliverables comply with regulatory requirements (e.g., FDA, EMA).

• Contribute to programming workflows, documentation, and best practices in version control.

• Support automation efforts and the development of R-based pipelines.

• Utilize SAS for legacy studies or in situations where SAS support is necessary.

⛳️ Requirements

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

• 4–6+ years of experience in clinical programming, with a strong emphasis on R.

• Demonstrated experience in creating SDTM and ADaM datasets using R.

• Familiarity with SAS programming.

• Strong understanding of CDISC standards (SDTM, ADaM).

• Experience with clinical trial data, regulatory submissions, and quality control processes.

• Excellent analytical, problem-solving, and documentation skills.

🏝️ Benefits

• Health insurance

• Competitive salary

• Flexible working hours