Sr Manager, Statistical Programming

Provides technical guidance and mentoring; Provides timely support to study teams on all programming matters according to product strategies; Performs, plans and coordinates project work to ensure timely, quality delivery across multiple projects; Contributes to strategic initiatives to improve departmental processes and scalability; Provides input into, or leads general standardization efforts (e.g., CRFs, query checks, standard statistical programs, data presentations); Assists in developing programming processes consistent with industry best practices; At least 8 years' industry (Pharmaceutical, Biotech, CRO) SAS programming experience or equivalent; At least 2 years management experience; Knowledge of clinical trials and experience in using SAS to report the results of clinical trials and/or integrated analysis for submission; Experience in constructing technical programming specifications and producing validated SAS programs Strong experience in working with CDISC standards, including SDTM, and ADaM and define documentation; Excellent knowledge of applied statistical methodologies; Excellent knowledge of SAS Macro, SAS/SQL, SAS/GRAPH, and SAS/STAT; Good communications and organizational skills required; Bachelor's Degree required, Master's Degree Preferred.