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The Associate Statistical Programming Director at IQVIA is responsible for leading statistical programming efforts to ensure submission-ready clinical data while managing a small team. The role requires extensive experience in clinical programming, specifically with SAS, and collaboration across various departments to meet regulatory obligations.
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Job Summary
Provide leadership and hands-on support in developing and maintaining statistical programming capabilities to meet regulatory obligations.
Responsible for the production of submission-ready data, tables, figures, listings, and submission packages, ensuring quality and accuracy.
Lead and oversee the design and implementation of complex SAS programs for clinical trial data analysis and reporting, including pooled and exploratory analyses.
Matching Summary
Match Score: 75
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The Associate Statistical Programming Director at IQVIA is responsible for leading statistical programming efforts to ensure submission-ready clinical data while managing a small team. The role requires extensive experience in clinical programming, specifically with SAS, and collaboration across various departments to meet regulatory obligations.
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Salary
Base: $98,200.00 - $273,200.00; Bonus/Equity: Incentive plans, bonuses may be offered; Benefits: Range of health and welfare and/or other benefits
Skills & Requirements
Must-have
SAS programming
CDISC SDTM and ADaM
submission ready data
clinical trial data analysis
SAS Macros development
regulatory requirements
Nice-to-have
leadership and team management
process improvement initiatives
cross-functional collaboration
solutions-oriented mindset
networking and knowledge sharing
Key Requirements
10+ years clinical/statistical programming experience
BSc in Computer Science, Mathematics, Statistics or related