ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialize in the strategic development, management and analysis of programs that support Clinical Development – from compound selection to Phase I - IV clinical studies ICON enjoys a strong reputation for quality and is focused on staff development.
We make it our mission to attract the most diverse and creative minds into the business and we continually strive to provide opportunities for our people to excel, grow and build a great career. We understand that our greatest asset is the skills and talents of our people and they are truly what set us apart.
Post: Central Monitor
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 RoleConduct 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.
Experience: Min., 1 year
Location: Chennai, Bangalore
Industry Type: Pharma/ Biotech/Clinical Research
Job Code: 043131
End Date: 9th Feb., 2017
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