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Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Senior Manager, Statistical Programming - **Company:** Travere Therapeutics, Inc. - **Location:** San Diego, CA, United States (Remote available) - **Experience:** Expert - **Salary:** $132,000.0 - $172,000.0 - **Contract:** Permanent contract - **Skills:** Microsoft Access, Microsoft Windows, Biometrics, Unix, Microsoft Office, Program Analysis, SAS (Software), Software Engineering, SQL Databases, Information Technology - **Published:** October 14, 2026 - **Apply:** https://travere.wd1.myworkdayjobs.com/TravereCareers/job/San-Diego/Senior-Manager--Statistical-Programming_R-100985 ## About the Role * Bachelor's degree in Statistics, Computer Science, Mathematics, or a related technical discipline required. Master's degree preferred. Equivalent combination of education and applicable job experience may be considered. * 7+ years' experience in clinical research required, ideally as a SAS programming for phase I-IV clinical trials in a pharmaceutical/CRO environment. Lead Programmer experience is required. * Technical knowledge and experience with SDTM, ADaM, and Define.XML. Additional Skills/Experience: * The ideal candidate will embody Travere's core values: Courage, Community Spirit, Patient Focus and Teamwork. * Driven, intelligent, passionate about making a difference for patients with rare diseases. * Strong understanding of the drug development process, submission-related activities and regulatory requirements (e.g. CDISC, CDASH, eCTD) and guidelines (eg, ICH, CHMP, FDA, GCP). * Experience in managing vendors and/or direct reports. * Demonstrated experience preparing and validating technical submission programming deliverables in accordance with applicable standards, procedures, and regulatory requirements. * Thorough knowledge of SAS functionalities (including ODS, SQL, MACRO, STAT, GRAPH, and ACCESS) and experience with MS Office are required. 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 effectively communicate and perform in a high demand and dynamic working environment. * Excellent communication skills and interpersonal skills. * Experience in solving complex and increasingly difficult problems by taking appropriate corrective action and implementing improvements. * Self-motivated and can independently manage responsibilities with minimal supervision. * Demonstrate initiative, sound judgement, and flexibility; possess effective time management and organizational skills; and capable of working on multiple projects simultaneously under tight timelines. * Ability to travel 10% domestically and internationally. * All positions have an essential job function to be able to perform face to face work with colleagues and/or onsite in San Diego. No role is expected to be 100% remote. ## Description The Senior Manager, Statistical Programming will work closely with the Associate Director, Statistical Programming and other members of the Biometrics team to provide programming support across all programs. The Senior Manager will independently plan and coordinate assigned programming activities, provide hands-on programming and validation support to project teams, and oversee external vendors to ensure timely and accurate deliverables. This role will also provide technical expertise to development programming standards and procedures and will work cross-functionally., * Provide strategic input regarding the development of statistical programming processes and contribute to maintaining programming-related SOPs, work instructions, and technical standards. * Assist in the development of programming standards and tools to improve the efficiency and accuracy required to support the analysis and reporting for clinical development projects. * Lead projects/studies, oversee contractors, and ensure quality and timeliness of programming deliverables. * Program analysis datasets, statistical tables, figures, listings, Integrated Summaries of Safety (ISS), Integrated Summaries of Efficacy (ISE), DSUR, PSUR, IB, progress reports, electronic submissions and other internal and external requests (e.g., publications, responses to regulatory questions). * Review/Develop CDISC specifications and review/generate SDTM data sets, ADaM data sets, and Define.xml files along with all supporting documentation for submissions. * Provide statistical programming and validation support for clinical study reports, oversee external vendors (e.g., CROs), and coordinate programming activities with Biometrics lead, data managers, and other study programmers. * Develop and/or review SAPs, case report forms, clinical DB specifications, validation plans, TLFs, reporting and analysis datasets specifications, and supporting documentation. * Provide input on the application of programming methodologies to support the clinical development process. * Additional duties assigned as need.