Statistical Analyst
Travere Therapeutics
August 21, 2026
Remote friendly (San Diego Metropolitan Area)
United States
Clinical Research and Development
Position Summary:
The Statistical Analyst will support biostatistics and clinical development activities across ongoing clinical studies, contributing to statistical analyses, data review, and high-quality study deliverables. Perform hands-on statistical programming, generate tables/listings/visualizations, support data quality and validation, and contribute to study documentation and exploratory analyses.
Responsibilities:
- Collaborate with biostatisticians and clinical development colleagues on clinical study analysis and data review.
- Perform statistical programming and generate summary tables, listings, and visualizations using SAS, R, or similar tools.
- Assist with quality control and validation of statistical deliverables for clinical study reports, publications, and presentations.
- Support exploratory data analysis and data cleaning.
- Contribute to development of statistical analysis plans (SAPs), study protocols, and study documentation under guidance.
- Participate in internal and cross-functional discussions.
- Provide statistical support to clinical studies/projects and execute analyses of clinical data.
- Apply statistical methodologies to turn data into actionable insights.
Education & Experience Requirements:
- Bachelor’s degree in Statistics, Biostatistics, Data Science, Mathematics, or related field required; Master’s preferred.
- 2+ years relevant experience in biopharmaceutical industry/healthcare system/related field required.
- Strong knowledge of fundamental statistical principles, best practices, and industry standards.
- Familiarity with clinical research statistical concepts (e.g., randomization, survival analysis, p-values, confidence intervals).
Additional Skills & Experience:
- Working knowledge of SAS or R; experience with clinical trial data or CDISC standards.
- Ability to explain statistical concepts to non-statisticians; strong communication/interpersonal skills.
- Ability to manage multiple tasks; attention to detail; detail-oriented and solution-driven.
- Working knowledge of drug development process; orphan/rare disease experience is a plus.
- Ability to travel ~5% and perform onsite/face-to-face work in San Diego (not 100% remote).
Benefits:
- Premium health, financial, work-life and well-being offerings; wellness/employee support programs; life insurance; disability; retirement plans with match; generous paid time off.
Compensation:
- Target base pay range: $85,000.00–$105,000.00.
Application Instructions:
- Accepting applications on an ongoing basis until a candidate is selected.
The Statistical Analyst will support biostatistics and clinical development activities across ongoing clinical studies, contributing to statistical analyses, data review, and high-quality study deliverables. Perform hands-on statistical programming, generate tables/listings/visualizations, support data quality and validation, and contribute to study documentation and exploratory analyses.
Responsibilities:
- Collaborate with biostatisticians and clinical development colleagues on clinical study analysis and data review.
- Perform statistical programming and generate summary tables, listings, and visualizations using SAS, R, or similar tools.
- Assist with quality control and validation of statistical deliverables for clinical study reports, publications, and presentations.
- Support exploratory data analysis and data cleaning.
- Contribute to development of statistical analysis plans (SAPs), study protocols, and study documentation under guidance.
- Participate in internal and cross-functional discussions.
- Provide statistical support to clinical studies/projects and execute analyses of clinical data.
- Apply statistical methodologies to turn data into actionable insights.
Education & Experience Requirements:
- Bachelor’s degree in Statistics, Biostatistics, Data Science, Mathematics, or related field required; Master’s preferred.
- 2+ years relevant experience in biopharmaceutical industry/healthcare system/related field required.
- Strong knowledge of fundamental statistical principles, best practices, and industry standards.
- Familiarity with clinical research statistical concepts (e.g., randomization, survival analysis, p-values, confidence intervals).
Additional Skills & Experience:
- Working knowledge of SAS or R; experience with clinical trial data or CDISC standards.
- Ability to explain statistical concepts to non-statisticians; strong communication/interpersonal skills.
- Ability to manage multiple tasks; attention to detail; detail-oriented and solution-driven.
- Working knowledge of drug development process; orphan/rare disease experience is a plus.
- Ability to travel ~5% and perform onsite/face-to-face work in San Diego (not 100% remote).
Benefits:
- Premium health, financial, work-life and well-being offerings; wellness/employee support programs; life insurance; disability; retirement plans with match; generous paid time off.
Compensation:
- Target base pay range: $85,000.00–$105,000.00.
Application Instructions:
- Accepting applications on an ongoing basis until a candidate is selected.