Senior Biostatistician

Travere Therapeutics

. Provide statistical support for assigned clinical studies under the guidance of the Biometrics/Biostatistics Team Lead or other senior statistical leadership .

Posted 11/6/2026full-timeSan Diego • California • United StatesSenior💰 $116,000 - $151,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in statistical methodologies and analysis within clinical trials, with proficiency in SAS programming and a solid understanding of FDA and ICH requirements. Capable of collaborating effectively across cross-functional teams while managing responsibilities independently.

Highest-signal resume keywords

SAS ProgrammingStatistical AnalysisClinical Trial DesignFDA and ICH RequirementsBiostatistics

ATS Keywords

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Hard Skills

Statistical Analysis PlansPower and Sample-Size CalculationsLongitudinal Data AnalysisSurvival AnalysisStatistical ModelingSimulationsCDISC StandardsSDTMADaMStatistical Methodologies

Soft Skills

Strong Communication SkillsCollaboration SkillsAbility to Explain Statistical Concepts

Certifications & Qualifications

Master's Degree in StatisticsMaster's Degree in Biostatistics

Industry Keywords

Biopharmaceutical IndustryContract Research OrganizationClinical Research EnvironmentDrug Development ProcessClinical Study Reports

About the role

Key responsibilities & impact

Provide statistical support for assigned clinical studies under the guidance of the Biometrics/Biostatistics Team Lead or other senior statistical leadership
Collaborate with clinical, data management, statistical programming, and other cross-functional team members
Contribute statistical input to study design, protocol development, endpoint definition, and analysis planning
Prepare and review statistical analysis plans, case report forms, clinical database specifications, validation plans, table, figure, and listing shells, analysis dataset specifications, and related documentation
Perform statistical analyses, simulations, and ad hoc analyses
Review statistical outputs and supporting documentation for accuracy, consistency, and compliance with study requirements
Support timely delivery of study-level datasets, analyses, and reports with statistical programming and data management
Review statistical deliverables prepared by external vendors or contract research organizations and escalate issues as appropriate
Contribute statistical input to clinical study reports, regulatory documents, publications, presentations, and internal data requests
Identify and evaluate complex statistical or data-related issues and propose solutions with senior statisticians
Apply established statistical methodologies to clinical trial data to support interpretation and decision-making
Contribute to Biometrics standard operating procedures, work practice documents, templates, and technical standards
Perform additional duties as assigned

Requirements

What you’ll need

Master's degree in Statistics, Biostatistics, or related field is required; an equivalent combination of education and applicable job experience may be considered
2+ years of relevant statistical experience in the biopharmaceutical industry, contract research organization, or related clinical research environment
Hands-on experience supporting statistical activities for clinical studies
Knowledge of statistical principles and methods applicable to clinical trial design, conduct, analysis, and reporting
Experience with study designs, power and sample-size calculations, longitudinal data analysis, survival analysis, statistical modeling, or simulations
Working knowledge of FDA and ICH requirements and applicable industry standards for clinical trial analysis and reporting
Familiarity with CDISC standards, including SDTM and ADaM
Proficiency in SAS programming for statistical analyses and production or review of tables, listings, and figures
Familiarity with clinical trial documents and deliverables, including protocols, statistical analysis plans, clinical study reports, and analysis dataset specifications
General knowledge of the drug development process
Ability to independently manage responsibilities and meet timelines with minimal supervision
Strong communication and collaboration skills
Ability to explain statistical concepts clearly to non-statisticians
Ability to travel as needed, up to 10%
Ability to perform face-to-face work with colleagues or onsite in San Diego

Benefits

Comp & perks

Premium health, financial, work-life and well-being offerings for eligible employees and dependents
Wellness and employee support programs
Life insurance
Disability benefits
Retirement plans with employer match
Generous paid time off
Short-term incentive
Long-term incentive compensation in company stock