We are currently seeking CRA I to join our team in Hungary. This role will be home based. ## What You Will Do You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situations based upon clinical research standards. 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 or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure) - Six (6) months of clinical monitoring experience - Basic understanding of Regulatory Guidelines - Ability to work within a project team - Good planning, organization, and problem-solving skills - Good computer skills with good working knowledge of a range of computer packages - Works efficiently and effectively in a matrix environment - Valid Driver's License - Fluency in English as well as in Hungarian Learn more about our EEO & Accommodations request here.