Emerald Clinical Trials is seeking a highly organised Project Specialist to support Early Phase project management teams in delivering global clinical trials. You will manage study documentation, trackers, and cross-functional meetings, ensuring timelines, quality, and regulatory compliance.
Ideal candidates have a Life Sciences degree and 2–3 years of CRO or sponsor experience, with proficiency in CTMS, eTMF, and MS Office.
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📌 Hybrid Project Specialist — Early-Phase Clinical Trials (New South Wales)
🏢 Emerald Clinical Trials
📍 New South Wales
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