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...
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.
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