16 oct
|
Fortrea
|
Barcelona
Fortrea seeks a Clinical Research Associate to monitor study sites in Catalonia, Spain, ensuring adherence to ICH GCP and regulatory guidelines. You will conduct visits, review data, liaise with vendors, and help keep trial timelines on track. The role requires at least 2 years of independent monitoring, oncology experience preferred, fluent in Spanish and English, a university degree, and a valid driver’s license. Travel is expected as part of the job.
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📌 CRA II: Lead Site Monitoring & Study Management (Barcelona)
🏢 Fortrea
📍 Barcelona