Clinchoice Inc.

Clinchoice Inc.

Principal Data Scientist Consultant (R with CDISC)

United States · Principal

Sponsorship not specifiedDetected 120 days ago
GitData AnalysisData ScienceComputer VisionStatisticsComplianceFDA RegulatoryMedical DevicesSASProblem SolvingGxPBiostatistics

Stay score

odds of building a lasting career here

40Risky
Cap-exempt (no lottery)0
Sponsors this role90
Entry-level history0
PERM / green-card track0
Lottery odds40
Fits your clock70

Thin sponsorship signal and lottery-bound. A low-probability bet with your clock running. Prioritize cap-exempt roles and proven entry-level sponsors first.

Lottery odds assume a STEM candidate.

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Employer immigration record

from this employer's Department of Labor filings

Green-card follow-through: 90%

Of 10 labor certifications old enough to have been used, 1 expired without the employer filing the next step. Median time from filing to decision: 490 days.100% of their filings were for a worker who already held the job.Only certifications past the 180-day window are counted — recent ones cannot have expired yet.

Sourced from Department of Labor LCA, PERM and prevailing-wage disclosure data. Employer matching is by name, so figures may be split across an employer's legal entities. Absence of a filing means none appears in our copy of the data, not that none exists.

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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 Data Scientist Consultant to join one of our clients.

Responsibilities

  • Develop, validate, and maintain SDTM and ADaM datasets using R following CDISC standards.
  • Support TLF (Tables, Listings, Figures) generation in R or SAS as needed.
  • Collaborate with statisticians, data managers, and clinical teams to understand programming requirements.
  • Perform QC checks, reconcile data issues, and ensure deliverables meet regulatory expectations (e.g., FDA, EMA).
  • Support automation initiatives and R-based pipeline development.

Requirements

  • Bachelor's or Master's degree in Statistics, Computer Science, Mathematics, Life Sciences, or related field.
  • 4-6+ 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.
  • Experience with clinical trial data, regulatory submissions, and QC processes.
  • Utilize SAS for legacy studies or where SAS support is required.

Nice to have

  • Experience with R packages such as tidyverse, haven, pharmaverse (e.g., admiral, tidyCDISC), or other clinical programming toolkits.
  • Understanding of R Markdown, Shiny apps, or reproducible reporting tools.
  • Exposure to GxP validation, version control (Git), and automated workflows.
  • Experience working in a CRO or pharmaceutical environment.
  • 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.
  • Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.
  • Who will you be working for?

Company info

  • We are seeking a Principal Data Scientist Consultant with strong experience in R and a solid background in clinical programming.

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.