Central Monitor

Central Monitor

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** you will play a pivotal role in ensuring data quality, patient safety, and study integrity across the clinical development lifecycle.

**What You Will Do:**

As a Central Monitor, you will work cross-functionally with study teams to proactively identify, assess, and mitigate risks using advanced data analytics and central monitoring tools.

Key responsibilities include:

+ Facilitate risk assessment throughout the study lifecycle, ensuring proactive identification and management of study risks
+ Develop and maintain Central Monitoring Plans in collaboration with study teams
+ Support study start-up, conduct, and close-out activities,...

Ready to Apply?

Submit your application today and join our talented team at ICON Clinical Research.

Submit Application