IQVIA LLC is seeking a Programming Team Lead to plan and oversee the programming lifecycle for complex clinical studies. You will design advanced macros, tools, and process improvements to increase efficiency while ensuring high-quality outputs.
The role requires 3–5 years of statistical programming experience in clinical trials, robust SAS skills, CDISC knowledge, and leadership abilities. Collaboration with cross-functional teams is essential for delivering regulatory-compliant results.
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📌 Senior Clinical Programmer Lead - SAS & SDTM/ADaM (Surry Hills)
🏢 Iqvia
📍 Surry Hills
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