Clinchoice Inc.

Principal Data Scientist Consultant- R programmer (Remote)

United States · Principal

Sponsorship not specifiedDetected 26 days ago

PythonGitCI/CDMachine LearningData AnalysisData ScienceComputer VisionStatisticsEHR/EMRFDA RegulatoryMedical DevicesSASProblem SolvingGxPBiostatistics

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.

Company info

to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices.
Our employees are the most valuable company asset, and they are the fulcrum around which all ClinChoice activities are built, and close management and training are the core instruments to develop and maintain highly-qualified personnel.
The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology.
The success of these core values is evidenced by our low industry-average turnover rates.
ClinChoice is an equal opportunity employer.
We have based our success on attracting, developing, and promoting talent, guided by a commitment to diversity and inclusivity.

Visa & Work Authorization

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