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Central Monitor

ICON Public Limited Corporation

ICON is looking for a Central Monitor to be based in Chennai. The Central Monitor is responsible for listing review and central data analysis to support quality and risk...

ICON is looking for a Central Monitor to be based in Chennai. The Central Monitor is responsible for listing review and central data analysis to support quality and risk reviews of projects, by highlighting/escalating trends.

Job Responsibilities

As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needsConduct 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.Performs data entry of Clinical Data Analysis and Central Monitor analysis results for communication to the project team.Supports implementation of central monitoring activities by focusing on central monitoring of aggregated data. Facilitates site oversight and early decision making by the Clinical trial Managers by identifying risks trends to critical study processes and dataSupport the Clinical Data Analyst with the set-up of the analysis platform, listing and Central Monitoring working tools for Clinical Data Analysts, Central Monitors and CRAs.Support the Clinical Data Analyst with the preparation of the Quality Risk Review Meetings and overall inspection readiness. Attend project meetings where required. In studies not involving a Clinical Data Analyst, work independently for communication of central monitoring outputs and inspection readiness to the project team.In studies applying Central analysis, support the Clinical Data Analyst with the preparation, conduct and follow-up of the Central Monitoring meetings with CRAsOther duties as assigned

Skillset requirementsGood communication skillsScientific background: Experience of 1 year in Clinical Research environmentExcellent Technical skills: must be able to use several systems as ICOTrial / ICONIK / Firecrest / RAVE / OMR

Extract data and customize reports

Excel knowledge (pivot table - Vlook Up function)Able to follow instructionsGood Analytic skills

Ability to do analysis via review of data listing, study specific data set

Good decision maker

Job posted: 2020-12-11

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