Clinchoice Inc.

Clinchoice Inc.

Senior Statistical Programmer Consultant (Oncology) Remote

United States · Senior

Sponsorship not specifiedDetected 124 days ago
Computer VisionStatisticsClinical TrialsFDA RegulatoryMedical DevicesSASLeadershipCommunicationBiostatistics

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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 filing pattern in this occupation

Context, not a finding about this posting: of this employer's 6 green-card filings in this occupation, 100% were for a worker who already held the job.

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 Senior Statistical Programmer Consultant to join one of our clients.

Responsibilities

  • Lead programming activities for oncology clinical trials across multiple studies.
  • Develop, validate, and maintain SDTM and ADaM datasets following CDISC guidelines.
  • Provide SAS programming expertise to support complex data derivations and analyses.
  • Act as programming lead for assigned studies, managing timelines and deliverables.
  • Support integrated analyses including ISS/ISE.
  • Regulatory & Submission Support

Requirements

  • Bachelor's or Master's degree in Statistics, Computer Science, Mathematics, Life Sciences, or related field.
  • 8-12+ years of statistical programming experience in pharma/biotech or CRO.
  • Expert-level proficiency in SAS.
  • Strong understanding of CDISC SDTM and ADaM standards.
  • Experience supporting regulatory submissions and preparing submission-ready outputs.
  • Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.
  • We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.

Benefits

  • Work closely with Biostatistics, Data Management, Medical Writing, and Regulatory Affairs.

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?
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This listing is sourced directly from Clinchoice Inc.'s careers page and normalized into a canonical job model.