Clinchoice Inc.

Clinchoice Inc.

Principal Biostatistician for inhouse project (Permanent role)

United States · Principal

Sponsorship not specifiedDetected 135 days ago
GCPComputer VisionStatisticsComplianceProject ManagementClinical TrialsFDA RegulatoryMedical DevicesSASCommunicationMentoringBiostatistics

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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

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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 11 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

  • ClinChoice is a global full-service CRO committed to professional growth and a quality-driven "one-team" culture.
  • About ClinChoice ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies.

Responsibilities

  • Lead and provide statistical support for clinical studies, primarily within Immunology or any therapeutic areas
  • Act as the lead statistician on assigned studies, overseeing statistical strategy and deliverables
  • Collaborate with cross-functional teams including Clinical, Programming, Data Management, and Regulatory

Requirements

  • Strong experience in Oncology studies
  • SAS programming skills required (hands-on or strong working knowledge)
  • Experience working in a CRO and/or pharmaceutical/biotech environment

Nice to have

  • Experience leading Phase II-III clinical trials
  • Prior interaction with regulatory agencies
  • Experience mentoring junior statisticians or programmers
  • Once you have submitted your CV, you will receive an acknowledgement that we received it.
  • If you have the requirements we need, you will be invited for 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?
  • About ClinChoice

Company info

  • Statistical Analysis Plans (SAPs)
  • Analysis Database Specifications (ADS)
  • Statistical sections of clinical study reports
  • Review and interpret analysis outputs, ensuring accuracy, quality, and regulatory compliance
  • Provide guidance and oversight to statistical programmers as needed
  • Communicate statistical concepts, results, and risks clearly to both technical and non-technical stakeholders
  • Ensure adherence to regulatory standards (FDA, ICH, GCP) and company SOPs
  • MS or PhD in Statistics, Biostatistics, or a related field

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