CRA II - Slovakia

Location

Slovakia

Posted

73 days ago

Salary

0

Seniority

Mid Level

Job Description

CRA II - Slovakia

Fortrea

We are recruiting for an experienced CRA to join our team in Slovakia (Bratislava/western part of the country). Key Responsibilities - 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). - Ensure subject safety, protocol compliance, and data integrity through thorough source data verification, eCRF review, query management, and oversight of informed consent processes. - Maintain inspection‑ready sites by ensuring completeness and accuracy of site regulatory documentation, eTMF, and investigational product accountability. - Collaborate closely with study teams to deliver milestones on time, support audit readiness, and address site issues proactively. Requirements - University degree or allied health qualification (e.g. nursing); equivalent relevant experience will be considered. - Minimum 2 years of independent clinical monitoring experience within clinical trials. - Strong working knowledge of ICH‑GCP, local regulatory requirements, and clinical monitoring processes. - Ability to work autonomously with minimal supervision in a matrix environment; strong planning and problem‑solving skills. - Fluent in English (written and spoken) and Slovak; willingness to travel up to 60% as required. Learn more about our EEO & Accommodations request here.

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