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