Principal Statistical Programmer (Clinical Trials)

The Principal Stat Programmer plays a critical role in ensuring the accuracy and integrity of statistical programming across various clinical projects. Key responsibilities include developing and validating complex data sets and outputs, collaborating with cross-functional teams, and providing technical guidance on statistical methodologies and programming best practices.

Requirements

• Develops and validates complex datasets and outputs using SAS programming, ensuring compliance with CDISC standards
• Collaborates with cross-functional teams to optimize statistical programming processes
• Provides technical guidance and expertise on statistical methodologies
• Mentors and guides junior programmers
• Contributes to the continuous improvement of programming workflows and departmental standards
• Ensures high-quality deliverables from the statistical programming department
• Leads initiatives to enhance programming tools and techniques
• Partners with leadership to align programming objectives with larger organizational goals