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ClinChoice

Principal Data Scientist Consultant

RemoteUnited States only
Published
Role
Data Science
Experience
Principal
Employment
Contract
Company size
Enterprise
Salary not disclosed
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Open to US only. Set where you work from to check your eligibility.

No BS summary

Principal Data Scientist / Clinical R Programmer for US remote contract work. Needs 2-3+ years in clinical programming, strong R, SDTM/ADaM datasets, CDISC standards, and working SAS knowledge.

Core skills

RSDTMADaM

Required skills

SASCDISC

Optional skills

tidyversehavenpharmaverseadmiraltidyCDISCR MarkdownShinyGit

What you'll do

  • Develop, validate, and maintain SDTM and ADaM datasets using R following CDISC standards.
  • Support TLF 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 such as FDA and EMA.
  • Contribute to programming workflows, documentation, and version control best practices.
  • Support automation initiatives and R-based pipeline development.
  • Utilize SAS for legacy studies or where SAS support is required.

What they require

  • 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 in creating SDTM and ADaM datasets using R.
  • Working knowledge of SAS programming.
  • Solid understanding of CDISC standards including SDTM and ADaM.
  • Experience with clinical trial data, regulatory submissions, and QC processes.
  • Strong analytical, problem-solving, and documentation skills.
  • Preferred: Experience with R packages such as tidyverse, haven, pharmaverse, admiral, tidyCDISC, or other clinical programming toolkits.
  • Preferred: Understanding of R Markdown, Shiny apps, or reproducible reporting tools.
  • Preferred: Exposure to GxP validation, version control, and automated workflows.
  • Preferred: Experience working in a CRO or pharmaceutical environment.

Benefits

  • Security and additional career opportunities from working for a global CRO.
  • Continuous training to develop and maintain qualified personnel.

ClinChoice is a partner to pharmaceutical, medical device, and consumer care innovators, providing expertise in clinical operations, biometrics, regulatory affairs, pharmacovigilance, medical affairs, and toxicology to support healthcare advancement and regulatory compliance.

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