EyeBio is seeking a Clinical Research Associate II to lead site monitoring and ensure protocol adherence across multiple sites as part of our clinical trials program.
The role focuses on maintaining high-quality data, safety, and regulatory compliance while fostering robust investigator relationships.The position requires advanced English proficiency and experience in ICH-GCP, with extensive travel (approximately 75%).
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📌 Clinical Research Associate Ii — On-Site Monitoring Lead (Queensland)
🏢 EyeBio
📍 Queensland
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