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](https://careers.fortrea.com/us/en/eeo-and-accommodations).