04 nov
|
Fortrea
|
Buenos Aires
04 nov
Fortrea
Buenos Aires
Fortrea is seeking a Regulatory Affairs professional to act as the primary site liaison, ensuring timely collection and submission of essential documents for EC/IRB/Regulatory Authority approvals.
You will support in-country regulatory activities, maintain compliant study documentation, and coordinate with vendors to meet general requirements.
Experience with ICH/GCP, regulatory guidelines, and CTIS submissions is preferred.
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📌 Regulatory Submissions Associate - Clinical Start-Up (Buenos Aires)
🏢 Fortrea
📍 Buenos Aires