Senior Biostatistician
Travere Therapeutics
August 21, 2026
Remote friendly (San Diego Metropolitan Area)
United States
Clinical Research and Development
Position Summary:
The Senior Biostatistician will provide statistical support to Health Economics and Outcomes Research (HEOR), Real World Evidence (RWE), and Market Access activities in support of drug development and commercialization.
Responsibilities:
- Provide statistical support to clinical studies/projects under senior Biostatistics leadership.
- Collaborate with cross-functional teams for HEOR, RWE, and Market Access.
- Plan and execute analyses of clinical trial data, claims databases, electronic medical records, disease registries, and other epidemiological sources.
- Identify statistical issues and propose solutions with study/project teams.
- Provide statistical input to study reports, value/reimbursement dossiers, publications, and other data requests; perform modeling/analyses.
- Prepare/review analysis plans, CRFs, database specifications, validation plans, TFL shells, analysis dataset specifications, and supporting documentation for observational studies/clinical trials.
- Review analytical work from colleagues, external collaborators, or vendors and escalate issues.
- Support timely, high-quality deliverables; contribute to Biometrics SOPs/technical standards.
- Apply statistical methodologies to generate actionable insights.
Education & Experience Requirements:
- Bachelor’s in Statistics/Biostatistics, Computer Science, Mathematics, Epidemiology, Health Economics, or related field (Master’s preferred).
- 4+ years relevant experience in biopharma or healthcare system.
- Strong HEOR/RWE/Market Access statistical principles; hands-on SDTM/ADaM and/or claims/EMR/registry data.
- Experience with study design, power/sample size, longitudinal/survival analysis, cost-effectiveness, modeling, simulation.
- Proficiency in R or SAS.
Additional Skills/Experience:
- Ability to collaborate (including with vendors/CROs); understanding of drug development process; rare disease/orphan disease a plus.
- Manage multiple timelines; communicate/statistical concepts to non-statisticians.
- Detail-oriented, solution-driven.
- Travel ~10% domestically/internationally; role not 100% remote.
Benefits:
- Premium health, financial, work-life/well-being offerings; wellness/support programs; life insurance; disability; retirement with match; generous paid time off.
Application Instructions:
- Travere will accept applications on an ongoing basis until a candidate is selected.
The Senior Biostatistician will provide statistical support to Health Economics and Outcomes Research (HEOR), Real World Evidence (RWE), and Market Access activities in support of drug development and commercialization.
Responsibilities:
- Provide statistical support to clinical studies/projects under senior Biostatistics leadership.
- Collaborate with cross-functional teams for HEOR, RWE, and Market Access.
- Plan and execute analyses of clinical trial data, claims databases, electronic medical records, disease registries, and other epidemiological sources.
- Identify statistical issues and propose solutions with study/project teams.
- Provide statistical input to study reports, value/reimbursement dossiers, publications, and other data requests; perform modeling/analyses.
- Prepare/review analysis plans, CRFs, database specifications, validation plans, TFL shells, analysis dataset specifications, and supporting documentation for observational studies/clinical trials.
- Review analytical work from colleagues, external collaborators, or vendors and escalate issues.
- Support timely, high-quality deliverables; contribute to Biometrics SOPs/technical standards.
- Apply statistical methodologies to generate actionable insights.
Education & Experience Requirements:
- Bachelor’s in Statistics/Biostatistics, Computer Science, Mathematics, Epidemiology, Health Economics, or related field (Master’s preferred).
- 4+ years relevant experience in biopharma or healthcare system.
- Strong HEOR/RWE/Market Access statistical principles; hands-on SDTM/ADaM and/or claims/EMR/registry data.
- Experience with study design, power/sample size, longitudinal/survival analysis, cost-effectiveness, modeling, simulation.
- Proficiency in R or SAS.
Additional Skills/Experience:
- Ability to collaborate (including with vendors/CROs); understanding of drug development process; rare disease/orphan disease a plus.
- Manage multiple timelines; communicate/statistical concepts to non-statisticians.
- Detail-oriented, solution-driven.
- Travel ~10% domestically/internationally; role not 100% remote.
Benefits:
- Premium health, financial, work-life/well-being offerings; wellness/support programs; life insurance; disability; retirement with match; generous paid time off.
Application Instructions:
- Travere will accept applications on an ongoing basis until a candidate is selected.