CRA 2 - Iqvia Biotech- Czech Republic
IQVIA · Prague, Czechia
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Role summary
Clinical Research Associate supporting biotech studies in Prague. Responsibilities include conducting site monitoring visits, managing recruitment and enrollment tracking, ensuring protocol compliance and regulatory adherence, maintaining trial documentation, and communicating with study sites. Requires a scientific or healthcare degree, at least one year of on-site monitoring experience, GCP/ICH knowledge, and fluency in Czech and English.
Privacy & handoff
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