Central Monitor in LATAM

IQVIA · São Paulo, Brazil +5 more

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Clinical OperationsFull-timeCompany career page

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Role summary

IQVIA seeks a Central Monitor to support clinical trials across Latin America from a remote location. The role involves centralized monitoring activities, data quality review, site interactions, and management of study documentation across multiple projects.

What they're looking for

Bachelor's degree in life sciences, related field, or nursing qualification
Minimum 2 years of clinical monitoring experience (onsite or remote)
Advanced proficiency in Excel
Advanced English language skills

What you'll be doing

Perform centralized monitoring activities and evaluate study data quality against protocol and regulatory requirements
Manage triggers, i-site packs, internal systems, and project-specific databases and tracking tools
Conduct subject-level data reviews to verify accuracy of inclusion/exclusion criteria, safety data, labs, and endpoints
Interact with sites and clinical research associates to address data issues and track study milestones
Participate in study team meetings and escalate quality issues to senior monitoring staff

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