Principal SAS Macro Developer

JD for Principal Macro Developer Clinvia LLC is a data science and technology company providing services in Clinical development to leading pharmaceuticals and biotech companies. Clinvia team is looking for SAS Macro Developer with a strong background in clinical trials and oncology studies. The ideal candidate will be responsible for developing and maintaining reusable SAS macros, tools, and utilities that streamline the creation of analysis datasets (ADaM), tables, listings, and figures (TLFs) in accordance with CDISC standards and oncology-specific reporting requirements. Key Responsibilities: Design, develop, validate, and maintain SAS macros to automate and standardize programming activities across oncology trials. Collaborate with statistical programmers, biostatisticians, and data managers to understand study requirements and deliver scalable SAS solutions. Ensure compliance with CDISC (SDTM/ADaM) , and support regulatory submissions (e.g., FDA). Create and maintain macro libraries used for generating ADaM datasets, TLFs, and data listings specific to oncology studies. Implement unit testing, version control, and documentation best practices for macros. Troubleshoot and optimize legacy SAS code and macros for efficiency and robustness. Participate in code reviews and quality checks. Support programming leads and project teams in oncology therapeutic area development. . Able to develop and validate Global Macro’s. Experience in Oncology domain Required Qualifications: Bachelor’s or Master’s degree in Computer Science, Life Sciences, Statistics, or related field. 10+ years of experience in SAS programming in the pharmaceutical or CRO industry. Minimum 8+ years of experience developing SAS macros in a clinical setting. Strong understanding of SDTM and ADaM standards. Hands-on experience with oncology study data and endpoints (e.g., RECIST, PFS, OS). Experience with statistical programming environments and tools (e.g., SAS/Base, SAS/Macro, SAS/Graph). Good understanding of regulatory requirements and clinical trial processes. Preferred Qualifications: Experience with Pinnacle 21, Define-XML, and other validation tools. Familiarity with safety and efficacy data analysis specific to oncology. Job Type: Contract Pay: From $140,000.00 per year Benefits: 401(k) Dental insurance Health insurance Vision insurance Schedule: 8 hour shift Day shift Monday to Friday Application Question(s): Have you worked in Phase 2/3 studies ? Have you worked in Pharma/Biotech/CRO as SAS Macro Developer? Minimum 7+ years of experience is required in Pharma. Work Location: Hybrid remote in Redwood City, CA 94063 Job Type: Contract Pay: From $140,000.00 per year Benefits: 401(k) Dental insurance Health insurance Vision insurance Work Location: Remote