ICON plc is a world-leading healthcare intelligence and clinical research organization. We foster an inclusive environment to shape the future of clinical development.
n
You will lead clinical trial monitoring tasks with a focus on quality and continuous improvement, traveling up to 60% to monitor sites and drive compliance. You will collaborate with cross-functional teams, provide training to staff, and build robust relationships with site personnel to ensure successful trial execution and data
📌 Senior Clinical Research Associate: Site Monitoring Lead (New South Wales)
🏢 ICON Strategic Solutions
📍 New South Wales
Reply to this offer
Impress this employer describing Your skills and abilities, fill out the form below and leave Your personal touch in the presentation letter.