Responsible for designing new programming standards and implementing them across the programming organization
Take full ownership of existing shared codebases and automation frameworks
Architect scalable reusable macro frameworks and modernize legacy code
Ensure consistent, efficient, and compliant programming practices aligned with CDISC and regulatory expectations
Collaborate with data management, statistics, clinical, and quality teams to ensure programming practices align with CDISC standards

BSc in Computer Science, Mathematics, Statistics or related area with relevant experience
10+ years of experience in clinical programming and/or statistical programming within the CRO/pharmaceutical environment using SAS Software
Expert-level SAS programming with advanced macro development capability (required)
Strong understanding of CDISC principles and working within regulated clinical development environments
Familiarity with additional scripting or analytical tools (e.g., R or Python) is beneficial

Associate Director, Programming – Macros & Automation

Key skills