Clinical Research Associate I

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.

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