Statistical Programmer

A company is looking for a Statistical Programmer. Key Responsibilities Provide programming support for Phase 1 to Phase 3 studies, including project integration and disease monitoring Create and review annotated CRF to SDTM datasets and ensure timely project deliverables Collaborate with various departments to enhance communication and promote process improvements Required Qualifications Master's Degree in Statistics, Computer Science, Mathematics, Engineering, or related discipline 1-5 years of clinical trial programming experience in the biotechnology or pharmaceutical industry Advanced SAS programming skills and experience with statistical software such as R and S-Plus In-depth knowledge of CDISC, including SDTM, ADaM, and controlled terminologies Strong organizational skills with the ability to prioritize tasks effectively