Principal Statistical Programmer/Analyst Consultant Remote

📋 Description Participate in CRF design, database review, data management plan, and data listings review Produce data listings, summary tables, and graphics for interim and final analyses Integrate data across studies; test, document, and validate programs per guidelines Coordinate data transfer and programming standards with CROs and vendors; validate TFLs Collaborate with Biometrics for clinical trial data analysis Execute ad-hoc requests, manuscripts, posters, and presentations 🎯 Requirements Min 10 years SAS programming in pharma/biotech; degree in CS, statistics, math Expert SAS programming, reporting, and validation standards Therapeutic area: Rare Disease CDISC data standards experience required Senior statistical programmer in FDA-regulated pharma/CRO Experience with Clinical Study Reports and NDA submission Ability to work on multiple tasks and meet deadlines Excellent verbal/written and interpersonal skills for cross-functional teams 🎁 Benefits Global full-service CRO with focus on quality and professional development Client-facing role with autonomy and high-trust relationships 28+ years in industry; 4,000 professionals in 20+ countries Equal opportunity employer with diversity and inclusivity