Clinical Research Associate II - France
Fortrea
Date: il y a 1 jour
Type de contrat: Temps plein
À distance
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
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!
[email protected]
;40
Learn more about our EEO & Accommodations request here.
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.
- 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.
- 1+ years of experience in medical, clinical, pharmaceutical, or related fields.
- Local project coordination or project management experience.
- 60-80% overnight travel, valid driver’s license required.
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!
[email protected]
;40
Learn more about our EEO & Accommodations request here.
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