Principal SAS Programmer

Advanced Clinical is a clinical development and strategic resourcing organization committed to providing a better clinical experience across the drug development journey. Our goal is to improve the lives of all those touched by clinical research – approaching each opportunity with foresight, character, resilience and innovation. Based on decades of experience, we help our clients achieve better outcomes by conducting candid conversations and anticipating potential issues through our customized solutions, providing the expertise and resources needed to bring life-changing therapies to the world. We are looking for a Principal SAS Programmer to join our growing team! **Responsibilities:** * Develop, maintain, and validate SAS programs for clinical trial data analysis, reporting, and submission purposes. * Lead the programming efforts for assigned clinical trials, ensuring high-quality deliverables. * Collaborate with statisticians, clinical data managers, and other team members to understand project requirements and ensure data integrity. * Create and maintain SAS datasets, including the generation of SDTM and ADaM datasets. * Develop and validate statistical tables, listings, and figures (TLFs) using SAS programming. * Ensure compliance with regulatory guidelines (e.g., FDA, EMA) and company SOPs. * Provide technical expertise and mentorship to junior programmers. * Participate in the development and review of study protocols, statistical analysis plans (SAPs), and other study-related documents. * Troubleshoot programming issues and provide solutions in a timely manner. * Stay up-to-date with the latest SAS programming techniques and industry best practices. * May be required to perform other duties as assigned. **Qualifications:** * Bachelor's or Master's degree in a related field (e.g., Statistics, Computer Science, Biostatistics). * Minimum of 8 years of experience in SAS programming within the pharmaceutical or CRO industry. * Strong understanding of clinical trial data and the drug development process. * Expertise in SAS programming languages (Base SAS, SAS/STAT, SAS/GRAPH, SAS/MACRO). * Experience with SDTM and ADaM datasets. * Experience in developing TLFs. * Knowledge of regulatory guidelines (e.g., FDA, EMA) and industry standards. * Excellent communication, interpersonal, and problem-solving skills. * Ability to work independently and as part of a team. * Proven ability to lead and mentor junior programmers. * Demonstrated ability to manage multiple projects simultaneously. Advanced Clinical is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.