• Bachelor’s, Master’s in Statistics, Biostatistics, Computer Science, Mathematics, or a highly related Scientific discipline.
• 8+ years of statistical programing experience within a bio/pharma company, or clinical research organization (CRO).
• Advanced proficiency in SAS (including complicated data steps, Macro language, and commonly used analysis procedures (e.g., PROC FREQ, PROC REPORT, PROC SQL, and PROC MIXED).
• Comprehensive understanding of CDISC standards and experience generating regulatory package artifacts like define.xml and Reviewer's Guides (cSDRG, ADRG).
• Strong communication, analytical, and problem-solving skills, with excellent time management and the ability to independently manage multiple high-priority projects in a fast-paced environment.
• Excellent interpersonal skills and the ability to collaborate effectively as part of a cross-functional team.
• Demonstrated ability to work independently, communicate proactively, and deliver results effectively in a remote work environment