Fortrea is seeking a regulatory affairs professional to support study maintenance and site startup activities, ensuring investigator and regulatory documents meet EC/IRB/Regulatory Authority timelines.
With guidance from senior staff, you will develop awareness of applicable regulatory legislation and guidance in assigned countries.You will assist in compiling, submitting, and obtaining approvals for submission documents, liaising with vendors, and performing quality reviews to ensure readiness
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📌 Regulatory Start-Up Specialist - Clinical Trials (Xico)
🏢 Fortrea
📍 Xico