Senior Statistical Programmer/Analyst Consultant

📋 Description Lead statistical programming activities for clinical studies within the oncology therapeutic area Develop, review, and maintain high-quality SAS programs for SDTM, ADaM, Tables, Listings, and Lead programming activities for interim and final analyses, including complex efficacy and safety Work closely with Biostatisticians to understand statistical analysis plans, programming Develop and review programming specifications and ensure consistency with study protocols, SAPs Support the creation and validation of CDISC-compliant SDTM and ADaM datasets. 🎯 Requirements Bachelor's or Master's degree in Statistics, Biostatistics, Mathematics, Computer Science, or a Strong experience in clinical trial statistical programming, preferably within a CRO Significant experience working on oncology clinical trials. Basic or working knowledge of R programming is preferred. Experience supporting regulatory submissions. Strong proficiency in SAS programming, including Base SAS and relevant SAS procedures used for