Clin Res Assoc I

Fortrea; Paris; Sur place; EUR 42 000 - 52 000; Plein temps

Résumé du poste

Fortrea in Paris is seeking a CRA I to join our clinical research team. You will apply your clinical judgment to monitor trial sites, respond to emergencies, and ensure high standards of participant safety and data quality.

Your responsibilities include conducting site visits, managing regulatory documentation, overseeing eTMF and product accountability, and collaborating with study teams to meet milestones and audit readiness.

Qualifications

• University or college degree or allied health certification from an accredited institution.
• At least 1 month of clinical monitoring experience.
• Good understanding of regulatory guidelines and standards.
• Ability to work effectively within a project team in a matrix environment.
• Strong planning, organization, and problem-solving skills.
• Good computer skills and familiarity with common software packages.
• Valid Driver's License.
• Fluency in English.

Responsabilités

• Independently manage and monitor clinical trial sites in line with ICH-GCP and Fortrea SOPs.
• Ensure subject safety, protocol compliance and data integrity through source data verification and eCRF review.
• Maintain inspection-ready sites with regulatory documentation and investigational product accountability.
• Collaborate with study teams to meet milestones, support audit readiness, and address site issues proactively.

Connaissances

English fluency

Regulatory guidelines knowledge

Teamwork ability

Planning and organization

Problem solving

Driver's License

Formation

University or college degree or allied health certification

Description du poste

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.