Fortrea is seeking an experienced regulatory start-up professional to serve as a local expert for site activation and maintenance across countries.
You will collect, review, and prepare essential documents for regulatory submissions and ensure timelines align with project management and client expectations.You will guide new hires, liaise with EC/IRB/Regulatory Authorities, and help maintain high-quality documentation to ensure audit-readiness for studies in the region.
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📌 Global Clinical Start-Up Specialist (Xico)
🏢 Fortrea
📍 Xico