Clinical Research Associate I

Seeking a CRA I to join the team in Hungary, working remotely, to monitor and manage clinical trial sites, ensuring compliance and participant safety.

Location: Hungary

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