Jobs and Careers
AR
Senior SAS Programmer
ArdelyxUnited Statesfull_timeVerifiedPosted 3 Mar 2026
💰 $172,000/yr($140,000/yr – $172,000/yr)
About the role
Ardelyx is a publicly traded commercial biopharmaceutical company founded with a mission to discover, develop and commercialize innovative first-in-class medicines that meet significant unmet medical needs. Ardelyx has two commercial products approved in the United States, IBSRELA® (tenapanor) and XPHOZAH® (tenapanor). Ardelyx has agreements for the development and commercialization of tenapanor outside of the U.S. Kyowa Kirin commercializes PHOZEVEL® (tenapanor) for hyperphosphatemia in Japan. A New Drug Application for tenapanor for hyperphosphatemia has been approved in China with Fosun Pharma. Knight Therapeutics commercializes IBSRELA in Canada. Position Summary: The Senior SAS Programmer is responsible for applying advanced programming techniques to support the development and validation of statistical programs to be used for monitoring, analyzing, and reporting of Ardelyx’ clinical trial data for regulatory submissions and publications across multiple disease areas at Ardelyx. This position works closely with Biostatisticians, Data Managers, Clinical Trial Managers, and if necessary, Contract Research Organizations (CROs) and/or SAS programming consultants, to meet project deliverables and timelines for clinical data monitoring, analyzing, and reporting. Responsibilities:
- Serve as the Lead Programmer to be responsible for the timeline and quality of all statistical analysis deliverables
- Manage and oversee contractors and external vendors for SAS programming activities
- Complete projects while adhering to departmental procedures and practices, technical and industry standards and programming concepts and conventions during all aspects of work
- Participate in study statistical programming development and documentation to include datasets, tables, listings and graphs to meet project timelines
- Conduct thorough program verification and validation, troubleshoots technical issues, and ensures accuracy and reproducibility of SDTM, ADaM datasets and TLFs
- Ensure high-quality statistical programming documentation, including dataset specifications, validation plans, and traceability documents
- Work closely with the Lead Biostatistician to create analysis specifications and analysis outputs following the instructions provided in the Statistical Analysis Plan
- Assist in the preparation and distribution of reports to the project team members
- Participate in the development and review of SOPs, working instructions, and associated documents for SAS programming
- Perform other duties as necessary as assigned by management
- Bachelor’s degree, master’s degree preferred, in Statistics, Biostatistics, Computer Science or related field with 5 - 8 years of SAS programming or equivalent experience
- 3+ years of pharmaceutical clinical trial experience preferred
- Strong understanding of clinical trial data and extremely hands-on in data manipulation, analysis, and reporting
- Advanced knowledge of SAS including data steps, PROC’s, SAS MACRO and SAS GRAPH
- Experience with EDC and some Clinical Data Management packages
- Hands-on experience implementing SDTM and ADaM data standards
- Preferred experience managing contractors and/or external vendors
- Preferred experience working on FDA submissions
- Strong interpersonal skills, strong organizational skills with great attention to details and the ability to multitask, and excellent written communication skills
Apply for this role
Generate a tailored application kit with a matched cover letter, interview prep, and CV highlights — in under 60 seconds.
Apply Now →Generate Application KitFree account required — sign up in 30s