ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
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:
Your Profile:
You are a href="https://careers.iconplc.com/benefits">careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
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