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Central Monitor

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About the role

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This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. The Central Monitor is responsible for listing review and central data analysis to support quality and risk reviews of projects, by highlighting/escalating trends.

Overview of the role:
Conduct risk indicator analysis via review of data listing, study specific data sets and aggregated data, make independent and sound decisions on analysis results. This includes the review of several sources of operational, clinical and other type of data.

Facilitates site oversight and early decision making by the Clinical trial Managers by identifying risks trends to critical study processes and data

set-up of the analysis platform, listing and Patient Centric Monitoring working tools for Clinical Data Analysts, Central Monitors and CRAs.

In Patient Centric Monitoring studies, support the Clinical Data Analyst with the preparation, conduct and follow-up of the Patient Centric Monitoring meetings with CRAs.
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Day in the life

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Publish date

06/10/2026

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Why I Still Recommend the CTA Role After More Than 10 Years in Clinical Research Clinical Operations Manager Yordan Zahariev reflects on career growth, leadership and the opportunities a CTA role

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Discover Yordan's career journey at ICON and learn how a CTA role can open doors across clinical research.

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Building Careers Across Latin America

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06/04/2026

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After more than 20 years at ICON, Carolina Boari has witnessed the organisation's growth across Latin America while building a successful career of her own. Today, as Executive Director of Clini

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Hear from Carolina about her career journey at ICON.

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Sajna's Biometrics Career Journey

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05/26/2026

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From Data Management to Leadership For Sajna Basant, a career in Biometrics has always been about more than data. “Data is not just numbers,” she explains. “It represents real people, their health

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