Fortrea in Sydney, Australia, is seeking a Clinical Research professional to oversee site monitoring and site management for unblinded studies, ensuring compliance with SOPs and regulatory guidelines. Travel may be required.
The role includes monitoring site activities, maintaining study files, coordinating visits, liaising with vendors, and contributing to budgets and SAE follow-up. Fluent English, regulatory knowledge, and CTMS experience are essential. This is a full-time, in office position.
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📌 Unblinded CRA I: Impactful Site Monitoring (Sydney)
🏢 Fortrea
📍 Sydney
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