Sitero in Australia seeks a Senior CRA to lead site monitoring for multicenter trials across life sciences. You will be the primary contact for site personnel throughout the trial lifecycle, from start-up to closeout, ensuring compliance with ICH-GCP and study protocol.
Candidates should have at least three years of independently monitoring drug trials with a CRO and a science degree; CNS experience is preferred. The role includes 40 hours/week, travel, and in office work with flexible schedules.
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📌 Senior Clinical Research Associate — Site Monitoring Lead (Melbourne)
🏢 Sitero
📍 Melbourne
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