Senior Manager, Statistical Programming

Role: Senior Manager, Statistical Programming overseeing programming activities for clinical development studies at a biopharma company. Responsibilities: lead statistical programming for clinical trials, ensure timely analysis and creation of outputs for reporting, review CRFs, Statistical Analysis Plans, TLGs, and collaborate with CROs to ensure data accuracy and compliance; participate in SOP development and study team communications. Requirements: Master’s in Statistics, Mathematics, or related field; at least 5 years of experience in statistical programming within pharma, biotech, or CRO environments; strong SAS (Base SAS, SAS macros, ODS) and working knowledge of R; CDISC experience; excellent communication and project management skills. Preferred: experience supporting NDA/MAA submissions, working with CROs, and knowledge of clinical data analysis. HighValue: clinical data analysis, regulatory submissions, CRO oversight, CDISC standards, SAS and R expertise, 20% travel. WorkSetup: not specified, but role involves external vendor interaction.