CRA II - Slovakia

April 28, 2026 Auto Import

We are recruiting for an experienced CRA to join our team in Slovakia (Bratislava/western part of the country).<div>Key Responsibilities<ul><li>Independently manage and monitor clinical trial sites in line with ICH‑GCP, applicable regulations, Fortrea SOPs, and study protocols (including initiation, routine monitoring, and close‑out visits).</li><li>Ensure subject safety, protocol compliance, and data integrity through thorough source data verification, eCRF review, query management, and oversight of informed consent processes.</li><li>Maintain inspection‑ready sites by ensuring completeness and accuracy of site regulatory documentation, eTMF, and investigational product accountability.</li><li>Collaborate closely with study teams to deliver milestones on time, support audit readiness, and address site issues proactively.</li></ul>Requirements<ul><li>University degree or allied health qualification (e.g. nursing); equivalent relevant experience will be considered.</li><li>Minimum 2 years of independent clinical monitoring experience within clinical trials.</li><li>Strong working knowledge of ICH‑GCP, local regulatory requirements, and clinical monitoring processes.</li><li>Ability to work autonomously with minimal supervision in a matrix environment; strong planning and problem‑solving skills.</li><li>Fluent in English (written and spoken) and Slovak; willingness to travel up to 60% as required.</li></ul></div>Learn more about our <a href="https://careers.fortrea.com/us/en/eeo-and-accommodations" target="_blank" rel="noopener noreferrer">EEO & Accommodations request here</a>.

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