Assoc Principal Scientist Statistical Programming, Late-Stage (Non-Oncology) (Hybrid)

Role: Lead statistical programming for late-stage drug/vaccine clinical development projects, overseeing analysis and reporting deliverables from trials to regulatory submissions. Responsibilities: develop and validate analysis datasets, manage project plans and resources, coordinate global programming teams including outsource providers, and ensure compliance with SOPs and GxP standards. Requirements: Bachelor's or Master's in a relevant field, with 7-9+ years of SAS programming experience in clinical trials; expertise in SAS, CDISC standards (ADaM), and clinical data management concepts; experience with regulatory submissions at a leadership level. HighValue: focus on late-stage (Phases 2/3) drug/vaccine projects, global regulatory submission experience, familiarity with GenAI tools (Python, R), and leadership in complex programming projects. WorkSetup: hybrid with 10% travel; located in the US.