Principal Data Scientist Consultant, R, CDISC

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

📋 Description

• Develop, validate, and sustain SDTM and ADaM datasets utilizing R in accordance with CDISC standards.

• Assist in generating TLF (Tables, Listings, Figures) in R or SAS as required.

• Create efficient, reproducible, and well-organized 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 align with regulatory standards (e.g., FDA, EMA).

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

• Assist with automation projects and the development of R-based pipelines.

• Employ SAS for legacy studies or whenever SAS support is necessary.

⛳️ Requirements

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

• 4–6+ years of experience in clinical programming, emphasizing R.

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

• Familiarity with SAS programming.

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

• Experience with clinical trial data, regulatory submissions, and QC protocols.

• Strong analytical, problem-solving, and documentation abilities.

🏝️ Benefits

• Health insurance

• Professional development opportunities

• Flexible work arrangements