Senior Scientist, Statistical Programming, Late-Stage Oncology (Hybrid)

Role: Statistical Programmer supporting late-stage drug and vaccine clinical development within BARDS, focusing on analysis and reporting for global regulatory submissions and post-marketing. Responsibilities: develop, validate, and maintain analysis datasets, tables, listings, and figures; lead project plans and coordinate a global outsourcing team; serve as the primary programming contact across product lifecycle; ensure process compliance and deliverable quality. Requirements: BA/BS in relevant fields plus 5+ years or MS plus 3+ years SAS programming experience in clinical trials; expertise in SAS, CDISC standards (ADaM), and clinical data management concepts; effective communication and collaboration skills; experience with regulatory submissions, including electronic deliverables preferred. High-Value: late-stage drug/vaccine development, global regulatory environment, SAS, CDISC standards, project leadership, and cross-functional collaboration. WorkSetup: hybrid, with 10% travel.