ICON Clinical Research is seeking a Clinical Trial Associate in Australia to assist with the design and analysis of clinical trials and interpret complex medical data. You will work closely with your team and stakeholders to deliver high-quality trial work.
Your responsibilities include coordinating trials, maintaining regulatory submissions and study documentation, and supporting the creation of CRFs and informed consent forms while traveling up to 10% as required.
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📌 Clinical Trials Associate: Study Coordination & Compliance (Sydney)
🏢 ICON Clinical Research
📍 Sydney
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