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Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # (Senior) Principal Statistical Programmer - **Company:** Beone Medicines Ltd. - **Location:** Emeryville, CA, United States - **Experience:** Expert - **Contract:** Permanent contract - **Skills:** Databases, Data Structures, SAS (Software), Macros, Information Technology, Data Management - **Published:** August 15, 2026 - **Apply:** https://dejobs.org/x/x/A229A86F813846B6BD27A3A667B2B71E/job/ ## About the Role * Expert-level SAS programming with experience delivering complex programming assignments and analyses. * Knowledge of SDTM and ADaM standards, including writing CDISC-standard dataset specifications and creating SDTM and ADaM datasets from specifications. * Ability to develop, test, and validate analysis datasets, tables, listings, graphs, macros, utilities, and presentation outputs. Other Qualifications: * Minimum 5+ years of clinical research and development programming experience using SAS. * Expert-level knowledge and extensive hands-on experience with CDISC methodologies. * Experience leading or working with centralized Statistical Programming teams. * Experience in oncology trials. * Experience with FDA, EMEA, and CFDA clinical trial and regulatory submissions. * Experience with the drug development process in preclinical, early, late-stage, and/or observational settings in related industries or academic research. * Knowledge of the drug development process and fundamentals of project planning and management. * Excellent verbal and written communication skills and the ability to collaborate effectively in a dynamic environment., Master's degree in Computer Science, Statistics, Mathematics, Life Sciences, or another relevant scientific subject, or equivalent related experience. ## Description The (Senior) Principal Programmer works within BeOne's Statistical Programming group to manage and support Statistical Programming deliverables for multiple clinical studies. The role serves as a technical lead and project manager, partners cross-functionally, and supports high-quality programming outputs for regulatory submissions, publications, and other clinical communications. Essential Functions of the Job: * Technically lead and project manage multiple studies, managing all aspects of study deliverables related to statistical and clinical programming, as needed. * Represent the Statistical Programming team at Study Management Team and Clinical Development meetings to address deliverables and timelines. * Assess resourcing needs and support adequate staffing of projects. * Assist in reviewing key study-related documents produced by other functions, including statistical analysis plans, case report forms, data management plans, database specifications, EDC data structures, DMC plans, and other clinical documents. * Interact and communicate with Statisticians, Data Managers, Clinical Operations, Medical Monitors, Medical Writing, and other partners to address programming-related study deliverables. * Write, test, and validate SAS programs to produce analysis datasets, tables, listings, graphs, and presentation outputs for regulatory submissions, publications, and other communications, as needed. * Understand and execute department-, product-, and study-level macros and utilities; write, test, and validate product- and study-level macros and utilities. * Serve as a technical resource for the programming group and provide advice on complex programming tasks and standards. * Contribute to the development and review of Statistical Programming policies, standard operating procedures, and other controlled documents. * Interface with outsourcing partners and vendors. * Perform other duties as assigned. Supervisory Responsibilities: Individual contributor role. No direct people-management responsibility is specified. 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