Allucent is seeking a Clinical Research Associate (CRA) hybrid role to independently monitor investigational sites, proactively identify issues, and ensure trials are conducted in line with protocols and GCP standards. You will lead monitoring activities and manage sponsor-site relationships, supporting regulatory affairs and startup processes.
The ideal candidate has 2+ years of onsite monitoring experience in complex trials, solid ICH-GCP knowledge, and explicit English communication.
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📌 Hybrid Clinical Research Associate: Site Monitoring Lead Perth
🏢 Allucent
📍 Perth
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