Offer summary

Qualifications:

Master’s Degree in Life Sciences or similar field., 3+ years of clinical monitoring experience, particularly in Oncology., Strong knowledge of regulatory and drug development processes., Fluent in local language and English with excellent communication skills..

Key responsabilities:

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

Manage site-level implementation of project plans and ensure audit readiness.

Verify adherence to protocols and regulatory requirements to ensure data integrity and patient protection.

Act as Lead CRA or Local Project Coordinator, overseeing site activities and mentoring new CRA staff.

Job description

Senior Clinical Research Associate (SRCRA )

Job Overview

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

As a SRCRA, 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:

Master’s Degree in Life Sciences or similar.
3+ years of clinical monitoring experience, including Oncology therapeutic areas.
Drive License mandatory.
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.

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!

micol.iafrate@fortrea.com

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