Clinical R Programmer Consultant (SDTM/ADaM Expert)

ClinChoice; United States; Remote; USD 90,000 - 120,000; Full time

Job summary

ClinChoice is seeking a Clinical R Programmer Consultant to join one of our client teams. The ideal candidate will develop SDTM and ADaM datasets in R, with SAS experience and CDISC standards knowledge, supporting regulatory submissions.

The role emphasizes collaboration with biostatistics and clinical data teams, delivering QCs and automated pipelines while ensuring regulatory compliance across FDA/EMA expectations.

Qualifications

• Bachelor’s or Master’s degree in Statistics, Computer Science, Mathematics, Life Sciences, or related field.
• 2–3+ years of experience in clinical programming with a strong focus on R.
• Proven experience 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.

Responsibilities

• 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 reporting.
• Collaborate with statisticians, data managers, and clinical teams to understand programming requirements.
• Perform QC checks, reconcile data issues, and ensure deliverables meet regulatory expectations.

Skills

R programming

Analytical thinking

Regulatory submissions

Education

Bachelor's or Master's in Statistics/CS/Life Sciences

Tools

SAS programming

Job description

ClinChoice is seeking a Clinical R Programmer Consultant to join one of our client teams. The ideal candidate will develop SDTM and ADaM datasets in R, with SAS experience and CDISC standards knowledge, supporting regulatory submissions.

The role emphasizes collaboration with biostatistics and clinical data teams, delivering QCs and automated pipelines while ensuring regulatory compliance across FDA/EMA expectations.