About this role
We are currently seeking CRA I to join our team in Paris.
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)
• 1 month 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
Learn more about our EEO & Accommodations request here.