Clinical Research Associate II - France

Fortrea; United States; Remote; USD 75,000 - 100,000; Full time

Job summary

Fortrea, une entreprise de recherche clinique dynamique, recherche un Clinical Research Associate II pour assurer des essais en oncologie. Le poste nécessite des compétences en monitoring clinique, gestion de sites et coordination de projets. Les candidats idéaux auront une expérience dans le domaine, des capacités exceptionnelles de communication, et seront prêts à travailler avec une équipe engagée, tout en participant à des recherches révolutionnaires qui améliorent la santé des patients.

Benefits

Package de rémunération compétitif

Programmes de santé et de bien-être

Opportunités de croissance professionnelle

Aménagements de travail flexibles

Qualifications

• 2+ ans d'expérience en monitoring clinique, y compris dans des domaines thérapeutiques en oncologie.
• Connaissance forte des processus réglementaires et du développement de médicaments.
• Compétences avancées en monitoring et gestion de sites.

Responsibilities

• Surveiller tous les aspects de la monitoring des sites d'étude et maintenir les fichiers d'étude.
• Gérer l'implémentation des plans de projet au niveau du site et assurer la préparation à l'audit.
• Agir en tant que contact principal pour les fournitures et fournisseurs d'essai clinique.

Skills

Clinical monitoring

Communication

Project coordination

Data integrity

Job description

Job Overview

Join Fortrea as a Clinical Research Associate II – Drive Clinical Excellence in Oncology Trials. This role is for upcoming future opportunities that may arise at Fortrea.

As a CRA II, you will ensure clinical studies are conducted to the highest regulatory and quality standards, protecting patient safety and delivering reliable data. You’ll coordinate designated clinical projects as a Local Project Coordinator and may act as a local client contact as assigned. Your work will help shape the future of clinical research and provide life-changing treatments to patients worldwide.

Summary Of Responsibilities

• Conduct all aspects of study site monitoring (pre-study, initiation, routine, closeout visits) and maintain study files.
• Manage site-level implementation of project plans and ensure audit readiness.
• Ensure data integrity and patient protection by verifying adherence to protocols, informed consent, and regulatory requirements.
• Monitor, review, and resolve data discrepancies, and generate accurate trip reports.
• Act as Lead CRA or Local Project Coordinator, overseeing site activities and project progress.
• Serve as point of contact for clinical trial supplies and vendors.
• Mentor and assist with the development of new CRA staff as assigned.
  
  

Qualifications

• 2+ years of clinical monitoring experience, including Oncology therapeutic areas.
• Strong knowledge of regulatory and drug development processes.
• Advanced site monitoring, site management, and registry administration skills.
• Fluent in local language and English, with excellent written and verbal communication.
  
  

Experience

• 1+ years of experience in medical, clinical, pharmaceutical, or related fields.
• Local project coordination or project management experience.
  
  

Work Environment

• 60-80% overnight travel, valid driver’s license required.
  
  

Benefits

At Fortrea, we value our team members and offer a comprehensive benefits package, including competitive compensation, health and wellness programs, and opportunities for professional growth. You’ll also enjoy flexible work arrangements and the chance to make a meaningful impact in cutting-edge clinical research.

Your Contribution To Fortrea’ s Success

In this role, you will help ensure the smooth execution of clinical trials and play a key role in delivering high-quality data and compliance. Your efforts will contribute directly to Fortrea’s mission of advancing clinical research and improving global health outcomes. Ready to make an impact? Join us!

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