07 Sep
|
Iqvia
|
New South Wales
07 Sep
Iqvia
New South Wales
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, solid SAS skills, CDISC knowledge, and leadership abilities. Collaboration with cross-functional teams is essential for delivering regulatory-compliant results.
J-18808-Ljbffr
📌 Senior Clinical Programmer Lead Sas & Sdtm/adam New South Wales
🏢 Iqvia
📍 New South Wales