Associate Centralized Monitoring Lead

IQVIA · Bratislava, Slovakia

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Clinical OperationsFull-timeCompany career page

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Role summary

This role supports centralized monitoring leads on clinical trial deliverables, ensuring data integrity and subject safety across assigned projects. Responsibilities include reviewing monitoring plans, developing analytics strategies, managing site metrics and performance trends, and collaborating with project teams to address clinical risks and optimize study quality. The position reports functionally to centralized monitoring leadership and operates within IQVIA SOPs and ICH/GCP guidelines.

What they're looking for

Bachelor's degree in clinical or life science discipline
Experience supporting centralized monitoring strategies and clinical risk assessment
Knowledge of ICH/GCP guidelines, protocol requirements, and regulatory compliance
Proficiency with study management plans, monitoring triggers, and analytics development
Ability to review site visit reports and identify data integrity issues
Experience with clinical trial operations and cross-functional project coordination

What you'll be doing

Support CMS leads on clinical deliverables across assigned projects from startup to closeout
Develop and oversee monitoring strategies including triggers, thresholds, and analytics proposals
Conduct periodic review of site-level KRIs and performance metrics to identify operational risks
Review subject-level clinical data and site visit reports; escalate issues to clinical leadership
Manage project resources and coordinate cross-functional teams to achieve study milestones

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Date posted30 days ago

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