SR Clinical Research Associate I - FSP Model - Home Based Italy
SR Clinical Research Associate I - FSP Model - Home Based Italy
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Job Description
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. Youll 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 lifechanging treatments to patients worldwide.
Summary of Responsibilities:
- Conduct all aspects of study site monitoring (prestudy initiation routine closeout visits) and maintain study files.
- Manage sitelevel 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:
- Masters Degree in Life Sciences or CRA certification (or 3 years relevant clinical research experience).
- 3 years of clinical monitoring experience including Cardiovascular and 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.
Experience:
- 1 years of experience in medical clinical pharmaceutical or related fields.
- Local project coordination or project management experience.
Work Environment:
- 6080 overnight travel valid drivers 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. Youll also enjoy flexible work arrangements and the chance to make a meaningful impact in cuttingedge clinical research.
Your contribution to Fortrea s success:
In this role you will help ensure the smooth of clinical trials and play a key role in delivering highquality data and compliance. Your efforts will contribute directly to Fortreas mission of advancing clinical research and improving global health outcomes. Ready to make an impact Join us!
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Learn more about our EEO & Accommodations request here.
Required Experience:
IC
Employment Type
Full-Time
