SrCRA Greece

Fortrea

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profile Job Location:

Athens - Greece

profile Monthly Salary: Not Disclosed
Posted on: 30+ days ago
Vacancies: 1 Vacancy

Job Summary

2026 will definitely be the year to join Fortrea!

To consolidate our FSO CRA Team in Athens we look forSenior Clinical Research Associate (SCRA).

Key Responsibilities:

  • Monitor Clinical Trials -conduct site visits to ensure compliance with protocols regulatory requirements and Good Clinical Practice (GCP) - National on sites visits in Greece

  • Site Management- Serve as the primary point of contact for investigational sites ensuring smooth study operations.

  • Source Document Verification (SDV)- Review and verify accuracy of clinical data collected from study sites.

  • Investigator Training and Support- Provide ongoing training to site staff on study protocols and regulatory requirements

  • Reporting and Documentation-Prepare monitoring reports maintain study records and contribute to overall trial documentation.

Qualifications:

  • Life Sciences University degreeorcertification in a related allied health professionfrom an appropriately accredited institution (e.g. nursing licensure).(Fortrea may consider relevant and equivalent experience in lieu of educational requirements)

  • Thorough understanding ofICH GCP Guidelinesand understanding oflocal regulatory requirements.

  • Thoroughknowledge of monitoring proceduresand basic understanding of the clinical trial process.

  • Fluency in English written and verbal.

What We Offer:

  • Remote position

  • Career growth environment in a supportive environment

  • Dedicated Line Manager

  • Works directly with a leading sponsor on innovative studies

  • Attractive salary and Fortrea benefits

If you are passionate about clinical research thrive in a collaborative environment and seek exciting career growth we want to hear from you!

Learn more about our EEO & Accommodations request here.

2026 will definitely be the year to join Fortrea! To consolidate our FSO CRA Team in Athens we look forSenior Clinical Research Associate (SCRA).Key Responsibilities:Monitor Clinical Trials -conduct site visits to ensure compliance with protocols regulatory requirements and Good Clinical Practice (G...
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