Clinchoice Inc.
Principal Data Scientist Consultant- R programmer (Remote)
United States · Principal
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About the role
- Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring?
- Our team says it's the best of both worlds...
- ClinChoice is searching for a Principal Clinical Data Scientist Consultant - R Programmer to join one of our clients.
Responsibilities
- Develop, validate, and maintain SDTM and ADaM datasets in R - using admiral and the broader pharmaverse - following CDISC standards.
- Perform Pinnacle21 validation, resolve findings, and refine specifications to ensure CDISC compliance and submission readiness.
- Partner with statisticians, data managers, and clinical teams to translate programming requirements into reliable deliverables.
- Perform QC, reconcile data issues, and ensure outputs meet regulatory expectations (e.g., FDA, EMA).
- Support automation, pipeline development, and version-controlled workflows.
- Use SAS for legacy studies or where SAS support is needed.
Requirements
- Bachelor's or Master's degree in Statistics, Computer Science, Mathematics, Life Sciences, or a related field.
- 5+ years in clinical programming, with a strong focus on R.
- Proven experience producing SDTM and ADaM datasets in R, including hands-on use of admiral.
- Experience with Pinnacle21 validation and remediation.
- Working knowledge of SAS programming.
- Working knowledge of Python for analytics, scripting, or tooling.
- Experience with clinical trial data, regulatory submissions, and QC processes.
- Generate Tables, Listings, and Figures (TLFs) in R or SAS as required by study needs.
Nice to have
- Broader pharmaverse experience (e.g., tidyCDISC, rtables) and tidyverse fluency.
- Exposure to AI/ML tooling in a clinical or programming context.
- Real-World Evidence (RWE) experience - e.g., mapping Flatiron or claims/EHR data into CDISC-aligned structures.
- R Markdown, Quarto, or other reproducible reporting workflows.
- GxP validation, Git-based version control, and CI/CD or automated workflows.
- CRO or pharmaceutical industry experience.
- Once you have submitted your CV, you will receive an acknowledgement that we have received it.
- If you have the requirements we need, you will be invited for a phone interview as the first step.
Visa & Work Authorization
- Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring?
This listing is sourced directly from Clinchoice Inc.'s careers page and normalized into a canonical job model.