IQVIA Inc. is seeking an Administrative Support specialist to assist CRAs and RSU teams with clinical documentation, TMF maintenance, and regulatory compliance. You’ll handle filing, archiving, and distribution of trial materials within project timelines.
The role requires solid English communication, MS Office proficiency, and solid organizational skills. Prior clinical trials experience and knowledge of GCP/ICH are advantageous, with in office responsibilities in North Sydney.
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📌 Clinical Trials Documentation & Compliance Assistant (Sydney)
🏢 IQVIA
📍 Sydney