Principal Statistical Programmer

Statistics & Data Corporation (SDC) is a specialized contract research organization (CRO) based in Arizona, offering top-tier clinical trial services to pharmaceutical, biologic, and medical device/diagnostic companies since 2005. SDC provides technology-enabled services to equip clients with the necessary clinical services expertise and technology for successful clinical trials. As a Statistical Programmer at SDC, your primary responsibility will be to provide statistical programming support for clinical trials. This includes generating and validating analysis datasets, tables, listings, and figures for clinical trials, creating SDTM mapping and datasets, and maintaining the infrastructure for project files of SAS datasets and SAS code. You will collaborate with Data Management on data set creations/transfers, integrity checks, and quality audits, and act as a liaison between clinical subcommittees and project teams as needed. Key responsibilities include: - Performing statistical programming for clinical trial analysis and reporting on large-scale, complex projects - Applying appropriate statistical methods for data analysis and providing expertise to project teams - Leading the design and development of SAS macros and utilities to expedite programming activities - Generating tables, listings, and figures per protocol and client requests - Reviewing reports for compliance with CDISC and FDA guidelines - Developing documentation and study data reviewers guides - Managing programming timelines, budgets, and client expectations - Mentoring junior statistical programmers and ensuring compliance with standard procedures and sponsor requirements Required skills for this role include strong analytical skills, proficiency in SAS programming (SAS/Base, SAS/Stat, SAS Macros, and SAS/Graph), problem-solving abilities, and the capability to work independently. You should also have excellent knowledge of statistical programming, the ability to communicate technical concepts clearly, and familiarity with clinical trial design and regulatory guidelines. To qualify for this position, you should have a Bachelor's degree in computer science, statistics, or a related field, along with at least eight years of relevant professional experience. Certification in SAS Base, Advanced, and Clinical Trials is preferred. At SDC, we are committed to developing our employees, offering growth opportunities, career advancement, a flexible work schedule, and engaging work culture. Our core values of Energy, Integrity, Engagement, Innovation, Ownership, and Commitment are central to our recognition program. Join our team to be part of a dynamic and innovative organization that supports both client and employee needs in the clinical research industry.,