04 ago
|
Worldwide
|
Argentina
04 ago
Worldwide
Argentina
Worldwide Clinical Trials is seeking a Specialist, Regulatory Compliance to perform quality review and approval of essential documents in compliance with the relevant Standard Operating Procedures, country regulations, and industry best practice prior to initiation of study sites. You will review the ED packages for completeness, communicate corrective actions, and track progress.
You will file electronic copies in the Trial Master File and work with Electronic Document Management Systems,
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📌 Global Regulatory Compliance Specialist (Argentina)
🏢 Worldwide
📍 Argentina