SR Clinical Research Associate I - FSP Model - Home Based Italy

FTITA Fortrea Development Limited Filiale Italiana; Milano; Remoto; EUR 40.000 - 60.000; Tempo pieno

Descrizione del lavoro

Join Fortrea as a Senior Clinical Research Associate (Sr. CRA) to drive clinical excellence in cardiovascular and oncology trials. You will ensure studies maintain high regulatory standards, coordinate clinical projects, and mentor new CRA staff, making a significant impact on global health.

Servizi

Competitive compensation

Health and wellness programs

Opportunities for professional growth

Flexible work arrangements

Competenze

• At least 3 years of clinical monitoring experience.
• Fluent in local language and English, strong communication skills.

Mansioni

• Conduct all aspects of study site monitoring.
• Manage site-level implementation of project plans.
• Ensure data integrity and patient protection.

Conoscenze

Monitoring

Project Coordination

Communication

Regulatory Knowledge

Site Management

Formazione

Master's Degree in Life Sciences

CRA Certification

Descrizione del lavoro

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.

Summary of Responsibilities :

• 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.

Qualifications :

• 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.

Experience :

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

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 will 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 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

Learn more about our EEO & accommodations request here.

Required Experience :

Key Skills: CSS, Cloud Computing, Health Education, Actuary, Building Electrician

Employment Type :

Full-Time

Experience :

Years

Vacancy :

1

Position :

Clinical Research Associate