Join Fortrea as a SR Clinical Research Associate2 - Drive Clinical Excellence in Neurology Trials.
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:
* 4+ years of clinical monitoring experience, mandatory experience in Neurology (preferably Ictus) therapeutic area.
* 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:
* 3+ 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!
micol.iafrate@fortrea.com
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