IQVIA in Australia is seeking an Administrative Support role to assist Clinical Research Associates and RSU in maintaining the Trial Master File and related clinical documentation.
The position involves handling, filing, and archiving documents to ensure site compliance within project timelines.Responsibilities include supporting document preparation, handling, distribution of study materials, and tracking CRFs and data flow.
A one-year contract with renewal potential, based on business needs.
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📌 Clinical Trial Documentation Coordinator (Victoria)
🏢 Iqvia
📍 Victoria
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