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