Clin Res Assoc I

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 .