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
Fortrea (Nasdaq: FTRE) is a leading global clinical research organization (CRO) dedicated to providing innovative clinical development solutions to the life sciences industry. With over 30 years of clinical research experience, Fortrea has evolved from Covance and Labcorp into a pureplay CRO built for biotech, biopharma, medical device and diagnostic innovators.
Fortrea collaborates with both emerging and established companies to deliver agile, fit-for-purpose full service (FSO), functional service (FSP) and hybrid solutions. Fortrea provides comprehensive Phase I-IV clinical trial management, clinical pharmacology, and consulting services, backed by deep experience in more than 20 therapeutic areas.
Operating in approximately 100 countries, our diverse and talented team brings scientific rigor, operational excellence, and a strong investigator site network to every trial. By combining the best of our legacy experience with forward-thinking innovation, Fortrea brings predictability to clinical trial execution and helps transform aspirations into outcomes.
Together, exceptional is possible.
Learn more at Fortrea.com
