Central Monitor - CluePoints

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

As a Central Monitor at ICON, you will ensure the quality and integrity of clinical trial data through centralized monitoring activities, contributing to the advancement of innovative treatments and therapies.

**What You Will Do:**

You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.

Key responsibilities include:

+ Conduct remote review and analysis of clinical trial data to identify trends, anomalies, and potential risks to patient safety and data quality.
+ Collaborate with site personnel and clinical teams to address findings from centralized monitoring activities...