IQVIA is seeking an entry-level Administrative Support role to assist the Clinical Research Associates (CRAs) and RSU team with maintaining trial master files and regulatory documentation.
The role involves handling, filing, and archiving study documents and supporting timely project delivery.
Responsibilities include assisting with study file reviews, clinical supplies tracking, data flow, and acting as a central communications contact.
Some in office support may be required after training.
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📌 Clinical Trials Documentation Specialist (Sydney)
🏢 Iqvia
📍 Sydney