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.