CRA 2 - IQVIA Biotech- Czech Republic

IQVIA · Prague, Czechia

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Clinical OperationsFull-timeCompany career page

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Role summary

Clinical Research Associate role focused on site monitoring and management for biotech studies in Prague. Responsible for conducting monitoring visits, managing recruitment, ensuring protocol compliance, and maintaining regulatory documentation across assigned study sites.

What they're looking for

Bachelor's degree in scientific or healthcare discipline, or equivalent education and experience
Minimum 1 year of on-site clinical monitoring experience
Strong knowledge of GCP and ICH guidelines
Proficiency in Microsoft Word, Excel, and PowerPoint
Fluent in Czech and English, written and verbal
Organizational and problem-solving abilities
Ability to build effective working relationships with sites and internal teams

What you'll be doing

Conduct site monitoring visits including initiation, ongoing monitoring, and close-out activities per protocol
Collaborate with sites on subject recruitment planning and track enrollment progress
Provide protocol training and maintain regular communication with study sites
Monitor CRF completion, data queries, and regulatory submissions
Maintain Trial Master File documentation and verify Investigator Site File compliance

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