What are the responsibilities and job description for the Senior Biostatistician position at Ardelyx?
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.
- Work closely with CROs and internal teams across the full trial lifecycle (start-up through close-out) to support trial execution activities and review biometrics deliverables, ensuring high-quality, traceable, and on-time outputs
- Review and contribute to key statistical documents (e.g., SAP, statistical monitoring plan, randomization specifications) and ensure alignment with protocol, study objectives, and regulatory expectations
- Oversee statistical analyses and ensure the accuracy and quality of statistical deliverables; partner with Statistical Programming on ADaM specifications, TLF shells, outputs, and QC
- Provide statistical input to clinical study design, including endpoints, estimands (as applicable), sample size and power calculation, randomization scheme, and analysis methodology
- Support the development of publications of Ardelyx study data, including performing ad hoc analyses, review abstracts, posters, and/or manuscripts, and responding to statistical/data-related questions from reviewers
- Contribute to regulatory filings and responses, e.g., supporting Regulatory for IND/NDA submissions, responding to statistical/data-related questions in FDA’s Information Request, and supporting PV for safety reporting including PADER and DSUR
- Collaborate with the Senior Manager, Biostatistics on statistical research projects and if needed, participates in cross-functional research projects
- Partner with Statistical Programming and Data Management to develop and maintain interactive dashboards that provide timely visibility into study progress and key metrics.
- MS or PhD degree in Biostatistics, Statistics, or related discipline with 2 - 7 years of relevant industry/CRO experience or equivalent experience
- Solid understanding of statistical methodologies, drug development process, regulatory requirements related to trial design, analysis, and reporting
- Experience with CDISC standards (SDTM/ADaM) and study-level statistical deliverables, including SAP development, TFL review/QC, and review of clinical or regulatory documents involving clinical trial data
- Proficiency working with statistical software; SAS experience strongly preferred. Experience with R/Python and data visualization tools (e.g., R Shiny, Tableau, Power BI) is a plus
- Strong written and verbal communication skills, with the ability to explain statistical concepts to non-statistical audiences
- Ability to establish and manage timelines, prioritize effectively and deliver accurate, high-quality biometrics outputs on schedule
Salary : $156,000 - $188,000