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ClinChoice

Senior/Principal Biostatistician Consultant

RemoteUnited States only
Published
Role
Data Science
Experience
Senior
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

Senior/Principal biostatistician consultant for clinical trials, focused on infectious disease programs such as Bronchiectasis or Hepatitis B. Requires MS or PhD in Statistics/Biostatistics, pharmaceutical or related clinical trials experience, and SAS/R programming. US remote contract role.

Core skills

SAS/RBiostatistics

Required skills

Poisson regression/Negative binomial methods/Time-to-event analysis/Multiple imputation methods

What you'll do

  • Serve as study statistician or support statistician on Bronchiectasis or Hepatitis B programs.
  • Develop protocols including study design, sample size calculation, randomization, and statistical analysis plans for assigned studies.
  • Provide statistical oversight to studies and ensure adequate quality and consistency with project requirements.
  • Ensure data for statistical analyses are complete, accurate, and consistent.
  • Own statistical analysis plans and the accuracy and timeliness of statistical input into reports or decisions.
  • Ensure validity of analysis and define alternative analysis strategies when unforeseen circumstances arise.
  • Apply extensive understanding of statistical concepts and methodologies.
  • Recognize and correct flaws in scientific reasoning and statistical interpretation.
  • Ensure accuracy and consistency of statistical tables, figures, data listings, report text, and consistency between summary tables and source tables/listings.
  • Own the statistical methods section for reports.
  • Identify and correct common flaws in interpretation of results, inconsistency in presentation or inference, adherence to report guidelines, and project-wide consistency.

What they require

  • MS or PhD in Statistics, Biostatistics, or related field.
  • High degree of technical competence.
  • Understanding of Poisson regression or negative binomial methods, time to event, or multiple imputation methods.
  • Competent in experimental design, descriptive and inferential statistics.
  • Pharmaceutical or related industry experience with clinical trials.
  • Preferred: Vaccines or infectious disease experience.
  • Excellent oral and written communication skills.
  • Excellent programming skills in SAS/R.
  • Ability to work independently while establishing a high-trust environment with client counterparts.
  • Confident candidate for a client-facing role.

Benefits

  • Work directly for a single sponsor while having the security and additional career opportunities of a global CRO.
  • Strong focus on quality, professional development, and supportive culture.
  • Continuous training to keep resources qualified in competence and expertise.
  • Below industry average turnover rates.

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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