Clin Res Assoc I

Fortrea; Paris; Sur place; EUR 42 000 - 56 000; Plein temps

Résumé du poste

Fortrea is seeking a CRA I to join our team in Paris. You will monitor clinical trial sites to ensure patient safety, protocol adherence and data integrity, while coordinating with study teams to meet milestones.

The role requires a healthcare degree or nursing licensure, at least 1 month of clinical monitoring experience, and fluency in English. A driver’s license is also required, and you will work within a matrix environment in a collaborative team setting.

Qualifications

• English fluency required.
• 1 month of clinical monitoring experience.
• Familiarity with regulatory guidelines.
• Ability to work within a project team.
• Strong planning, organization and problem-solving skills.
• Proficient in computer use and software packages.
• Driver's license required.

Responsabilités

• Independently manage and monitor clinical trial sites in line with ICH-GCP, regulations and Fortrea SOPs.
• Ensure subject safety, protocol compliance and data integrity through SDV, eCRF review, query management and informed consent oversight.
• Maintain inspection-ready sites with complete site regulatory documentation, eTMF and accountability of investigational products.
• Collaborate with study teams to meet milestones, support audits and address site issues proactively.

Connaissances

Fluency in English

Clinical monitoring

Regulatory guidelines

Team collaboration

Formation

Healthcare degree or nursing licensure

Outils

eCRF

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.