Ora’s Clinical Trial Associate I (CTA I) assists Project Managers and study teams in ophthalmic clinical research, supporting feasibility, site contracts, budgets, regulatory documents, and scheduling follow-up visits while ensuring compliance with GCP and study objectives.
The role covers start-up, maintenance, and close-out activities, documentation management in CTMS/eTMF, and collaboration across cross-functional teams; travel up to 10% and adherence to Ora’s values of kindness, operational
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📌 Ophthalmic Clinical Trial Associate I — Start-Up & Compliance (Australia)
🏢 Ora
📍 Australia