Clinical Research Associate II

Fortrea; Rueil-Malmaison; Sur place; EUR 40 000 - 60 000; Plein temps

Avantages offerts par ce poste

Competitive benefits

Flexible work model

Continuous learning and mentorship

Résumé du poste

A leading healthcare company in Île-de-France is seeking a Clinical Research Associate (CRA) to manage clinical trial sites and ensure regulatory compliance. In this role, you will monitor site activities, conduct data verification, and collaborate with teams to support innovative therapies. Candidates should have a relevant degree and strong understanding of ICH-GCP guidelines. This position offers the chance to influence global clinical research and benefit from a supportive work environment with flexible models and competitive benefits.

Qualifications

• Degree in life sciences, nursing, pharmacy, or related field.
• Strong understanding of ICH-GCP and regulatory requirements.
• Experience with clinical trial monitoring and data integrity.

Responsabilités

• Manage clinical trial sites according to SOPs and regulations.
• Conduct site monitoring visits ensuring protocol adherence.
• Perform source data verification and ensure data quality.

Connaissances

Attention to detail

Communication skills

Clinical trial processes

Regulatory compliance

Understanding of ICH-GCP

Fluency in English

Formation

University degree in life sciences or related field

Outils

Clinical systems and tools

Description du poste

Overview

Be the connection between science and solutions. In this CRA position, you’ll help transform complex clinical protocols into real-world results, working alongside a team that values precision, integrity, and progress. This role will offer you the opportunity to directly influence the success of global clinical trials and the delivery of innovative therapies to patients worldwide.

This role is for upcoming future opportunities that may arise at Fortrea

Responsibilities

• Manage clinical trial sites in alignment with Fortrea SOPs, ICH-GCP, project plans, and sponsor requirements, including oversight of training documentation and regulatory compliance.
• Conduct all phases of site monitoring visits (pre-study, initiation, routine, and close-out), ensuring subject safety, protocol adherence, and data integrity.
• Perform source data verification, query resolution, and eCRF review to ensure high-quality, audit-ready clinical data.
• Maintain and update essential documents in eTMF and sponsor systems, ensuring regulatory and documentation completeness throughout the study lifecycle.
• Monitor investigational product (IP) accountability, storage, and compliance with protocol and regulatory standards.
• Collaborate with cross-functional teams to align site performance with study timelines, metrics, and quality expectations.

Qualifications

• University or college degree in life sciences, nursing, pharmacy, or a related allied health profession; equivalent relevant experience may be considered in lieu of formal education.
• Solid understanding of ICH-GCP guidelines and local regulatory requirements governing clinical research.
• Working knowledge of clinical trial processes and monitoring procedures.
• Strong attention to detail and ability to follow complex protocols and documentation standards.
• Fluent in English both written and verbal.
• Proficient in using clinical systems and tools; able to work independently and travel as required.

Why Join Us?

• Contribute to advancing innovative therapies and improving patient outcomes through meaningful clinical research on a global scale.
• Thrive in a collaborative environment that values continuous learning, mentorship, and professional development.
• Work with modern clinical technologies and streamlined systems that support efficiency, quality, and compliance.
• Benefit from a flexible work model, competitive benefits, and a strong commitment to employee well-being.

We invite qualified candidates who are committed to excellence in clinical research to apply and become part of Fortrea’s mission to advance healthcare worldwide. If you are seeking a rewarding opportunity within a globally respected organization, we encourage you to submit your application today.