Clinical Monitoring Analyst

IQVIA

. Supports the Centralized Monitoring Lead (CML) in the development of the fit-for purpose CM strategy by contributing to the identification of the relevant CM elements to be implemented for the study (Quality Tolerance Limits (QTL), Key Risk Indicators, data visualizations and Data Quality Assessments) .

Posted 5/12/2026full-timeRemote • 🇬🇧 United KingdomMid-LevelSeniorWebsite

About the role

Key responsibilities & impact

Supports the Centralized Monitoring Lead (CML) in the development of the fit-for purpose CM strategy by contributing to the identification of the relevant CM elements to be implemented for the study (Quality Tolerance Limits (QTL), Key Risk Indicators, data visualizations and Data Quality Assessments)
Setup/Program QTL, KRI and Data Quality Assessments according to the study CMP
Refresh the Centralized Monitoring Platform at predefined frequency to enable signal identification
Generate and maintain the Centralized Monitoring Platform specifications document and file it in eTMF
Review and understanding of protocol is key

Requirements

What you’ll need

At least 3 years relevant experience in the area of pharmaceutical research and development or related field preferably in centralized Monitoring, data management, and/or biostatistics
2-3 years SAS experience including macro language
Knowledge/experience working on Cluepoints
Excellent command, both verbal and written, of English

Benefits

Comp & perks

Health insurance
401(k) matching
Professional development opportunities

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

SASmacro languagedata managementbiostatisticsdata visualizationsQuality Tolerance LimitsKey Risk IndicatorsData Quality AssessmentsCentralized Monitoringprotocol review

Soft Skills

verbal communicationwritten communication