Jobs in Ancona, Italy

Join Fortrea as a Senior Clinical Research Associate (Sr. CRA) and drive clinical excellence in cardiovascular and oncology trials. This role is for upcoming future opportunities that may arise at Fortrea.

As a Sr. CRA, you will ensure clinical studies are conducted to the highest regulatory and quality standards, protecting patient safety and delivering reliable data. You will 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.

• Conduct all aspects of study site monitoring, including pre-study, initiation, routine, and 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.

• Master's Degree in Life Sciences or CRA certification (or 3 years relevant clinical research experience).
• At least 3 years of clinical monitoring experience, including cardiovascular and oncology therapeutic areas.
• Strong knowledge of regulatory and drug development processes.
• Advanced skills in site monitoring, site management, and registry administration.
• Fluent in the local language and English, with excellent written and verbal communication skills.

• Minimum 1 year of experience in medical, clinical, pharmaceutical, or related fields.
• Experience in local project coordination or project management.

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 will also enjoy flexible work arrangements and the chance to make a meaningful impact in cutting-edge clinical research.

In this role, you will help ensure the smooth conduct 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!

Location : Remote

Job ID : LIM1;40

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Full-Time

Years

1

Position :

Clinical Research Associate