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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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