06 Sep
|
Iqvia
|
New South Wales
06 Sep
Iqvia
New South Wales
Job Description
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.
📌 Senior Clinical Programmer Lead - Sas & Sdtm/Adam (New South Wales)
🏢 Iqvia
📍 New South Wales