14 Sep
|
Iqvia
|
Melbourne
IQVIA is seeking a hands-on Programming Team Lead to plan, coordinate, and oversee programming activities for complex clinical studies. You will own the programming lifecycle from database integration to statistical outputs and design advanced macros and tools to improve efficiency.
The role requires 3–5 years of statistical programming experience in clinical trials, expert SAS (Base, Graph, Macro), and robust CDISC SDTM/ADaM knowledge.
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📌 Senior Clinical Stats Programmer: Lead & Innovate (Melbourne)
🏢 Iqvia
📍 Melbourne