CSL Ltd is seeking an Associate Director of Statistical Programming to lead the development and maintenance of statistical programming capabilities for clinical trials. The role requires extensive experience in clinical or statistical programming, particularly using SAS, and emphasizes collaboration, quality assurance, and innovation in programming processes
Job Summary
Provides leadership and expertise in driving the development and maintenance of statistical programming capabilities to meet regulatory obligations.
Oversees CRO delivery or manages in-house programming of data sets, outputs, and DDT files for clinical trials and integrated analysis.
Tests and implements state-of-the-art programming methods and tools, driving automation and AI integration.
Matching Summary
Match Score: 85
CSL Ltd is seeking an Associate Director of Statistical Programming to lead the development and maintenance of statistical programming capabilities for clinical trials. The role requires extensive experience in clinical or statistical programming, particularly using SAS, and emphasizes collaboration, quality assurance, and innovation in programming processes.
Skills & Requirements
Must-have
SAS Software expertise
SAS Macro language
CDISC standards knowledge
Clinical trial data analysis
Regulatory compliance
Nice-to-have
AI implementation
Automation of tasks
Cross-functional collaboration
Mentoring programmers
Senior management communication
Key Requirements
10+ years of experience in clinical/statistical programming
BSc in Computer Science, Mathematics, Statistics or related area