Associate Director, Statistical Programming

Role: Associate Director of Statistical Programming leading clinical trial data analysis and submission support. Responsibilities: provide technical and operational leadership in delivering high-quality programming for clinical studies and NDA submissions, develop and validate SAS and R programs, collaborate with Biostatistics, Data Management, and other functions on CDISC standards (SDTM, ADaM), manage internal and vendor programming support, and standardize processes. Qualifications: minimum 10 years’ SAS programming experience in Pharma/Biotech/CRO, experience managing programming teams, expertise in CDISC standards, proficiency in SAS/Base, SAS/Macro, SAS/STAT, SAS/Graph, SAS/SQL, and hands-on R programming skills; bachelor’s degree required, master’s preferred in computer science, statistics, or related fields. High-value: focus on clinical trial data analysis supporting NDA/BLA submissions, experience with CDISC standards, vendor oversight, and programming best practices. Work setup: U.S.-based, salary range $181,100–$244,900, with potential bonuses. The role emphasizes cross-functional collaboration, regulatory compliance, and process standardization in the context of biopharma clinical development.