(Senior) Principal Statistical Programmer

Role: (Senior) Principal Programmer within BeOne’s Statistical Programming group, leading and managing programming deliverables for multiple clinical studies. Responsibilities: serve as technical lead and project manager, oversee SAS programming for analysis datasets, tables, listings, graphs, and presentations for regulatory submissions; review study documents; collaborate with cross-functional teams including statisticians, data managers, and clinical operations; support study planning and resource allocation; ensure adherence to CDISC standards; interface with vendors and outsourcing partners; contribute to policies and SOPs. Requirements: minimum 5+ years of SAS programming experience in clinical research; expert-level SAS skills; extensive knowledge of CDISC standards (SDTM, ADaM); experience with oncology trials; familiarity with regulatory submissions to FDA, EMEA, and CFDA; strong communication and collaboration skills; Bachelor's or Master's in life sciences, computer science, statistics, or related field. Preferred qualifications include experience leading centralized programming teams and working across different drug development phases. High-Value: oncology indications, regulatory submission experience, CDISC expertise, preclinical to late-stage development. Work setup: not specified; travel requirements not mentioned.