30 sep
|
Worldwide Clinical Trials
|
Xico
30 sep
Worldwide Clinical Trials
Xico
Worldwide Clinical Trials seeks a regulatory start-up professional to manage end‐to‐end site activation for awarded projects.
You will coordinate regulatory submissions, essential document collection, and country‐specific requirements to support timely site initiation.Responsibilities include local liaison for regulatory activities, customization of country documents, risk assessment, and proactive communication with RAM and project teams to ensure milestones are met with quality and compliance.
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📌 Global Regulatory & Site Activation Specialist (Xico)
🏢 Worldwide Clinical Trials
📍 Xico