Emerald Clinical Trials is seeking a Clinical Research Associate 2 (CRA2) to join its Clinical Operations team. You will oversee site management, monitoring activities, and regulatory compliance across trials, ensuring high-quality execution and adherence to SOPs.
The role requires 2–5 years of on-site monitoring experience, robust knowledge of ICH‑GCP, and excellent communication and negotiation skills. A willingness to travel and work in a global context is essential.
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📌 Clinical Research Associate II — Australia (Adelaide)
🏢 Emerald Clinical
📍 Adelaide
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