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Travere Therapeutics

Senior Manager, Statistical Programming

Travere Therapeutics

. Provide programming support across all programs .

Posted 10/15/2026full-timeSan Diego • California • United StatesSenior💰 $132,000 - $172,000 per yearWebsite

Tech Stack

Tools & technologies
Google Cloud PlatformSDLCSQLUnix

About the role

Key responsibilities & impact
  • Provide programming support across all programs
  • Independently plan and coordinate assigned programming activities
  • Provide hands-on programming and validation support to project teams
  • Oversee external vendors to ensure timely and accurate deliverables
  • Contribute to programming-related SOPs, work instructions, and technical standards
  • Develop programming standards and tools to improve efficiency and accuracy for clinical development analysis and reporting
  • Lead projects and studies and ensure quality and timeliness of programming deliverables
  • Program analysis datasets, statistical tables, figures, listings, ISS, ISE, DSUR, PSUR, IB, progress reports, electronic submissions, publications, and regulatory responses
  • Review and develop CDISC specifications and review or generate SDTM, ADaM, and Define.xml files with supporting documentation
  • Provide statistical programming and validation support for clinical study reports
  • Coordinate programming activities with Biometrics leads, data managers, and study programmers
  • Develop and/or review SAPs, case report forms, clinical database specifications, validation plans, TLFs, reporting and analysis dataset specifications, and supporting documentation
  • Provide input on programming methodologies supporting the clinical development process
  • Work cross-functionally with Biometrics and other teams
  • Perform additional duties as assigned

Requirements

What you’ll need
  • Bachelor’s degree in Statistics, Computer Science, Mathematics, or a related technical discipline required
  • Equivalent combination of education and applicable job experience may be considered
  • Master’s degree preferred
  • 7+ years’ experience in clinical research required
  • Experience as a SAS programmer for Phase I-IV clinical trials in a pharmaceutical/CRO environment
  • Lead Programmer experience required
  • Technical knowledge and experience with SDTM, ADaM, and Define.XML
  • Strong understanding of the drug development process, submission-related activities, regulatory requirements, and guidelines, including CDISC, CDASH, eCTD, ICH, CHMP, FDA, and GCP
  • Experience managing vendors and/or direct reports
  • Experience preparing and validating technical submission programming deliverables
  • Thorough knowledge of SAS functionalities, including ODS, SQL, MACRO, STAT, GRAPH, and ACCESS
  • Experience with Microsoft Office
  • Familiarity or experience with R Software is a plus
  • Proven experience with UNIX and Windows operating systems
  • Understanding of the software development life cycle
  • Ability to travel 10% domestically and internationally
  • Ability to perform face-to-face work with colleagues and/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 (company stock)