Senior/Principal Statistical Programmer

📋 Description Serve as a lead statistical programmer for multiple studies and/or compounds, ensuring high-quality Lead and execute statistical programming activities across clinical trials, from study start-up Ensure consistency, quality, and executional excellence across programming deliverables for Support programming activities for global regulatory submissions and responses to health authority Provide technical oversight and guidance for outsourced statistical programming activities Develop, review, and validate high-quality statistical programming deliverables, including tables 🎯 Requirements Strong proficiency in SAS programming within a pharmaceutical, biotechnology, or CRO environment. Strong understanding of CDISC standards, including SDTM and ADaM. Hands-on experience with SDTM and ADaM specification, development, and programming. Strong experience in TFL programming and reporting. Experience supporting clinical trial reporting and/or regulatory submissions. Experience working with complex clinical trial data and study designs. 🎁 Benefits Working directly for a single sponsor while having the security and additional career opportunities Career opportunities within a global CRO