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· contribute to project coordination, progress reporting, meeting facilitation, and School‑level service activities that support the smooth operation of the research program · actively contribute to a
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trial management and coordination with extensive experience in clinical trial documentation and use of relevant software’s including but not limited to REGIS for ethics and governance submission processes
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‑resilient health systems · manage research ethics and governance processes, including trial registration, ethics submissions, amendments, and compliance reporting · contribute to national and
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governance processes, including ethics submissions, amendments, trial registration, and compliance with data governance and institutional requirements · contribute clinical insight, drawing on intensive
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organisational skills, with the ability to work effectively both independently and as part of a team be confident using computer applications including the Microsoft Office suite and online collaboration tools
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that enhances policy, practice, industry, and community outcomes · work effectively with multidisciplinary teams including clinicians, human factors experts, computer scientists, and AI experts
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image analysis a demonstrated ability to manage large and complex clinical research projects and oversee the project from start to end a demonstrated ability to effectively engage complex stakeholder
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design, ensuring quality, transparency, and excellence in all research activities · oversee ethics and governance processes, including trial registration, ethics submissions, amendments, and ongoing
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. Strong planning, organisational, computer literacy, and interpersonal skills, with the ability to manage competing priorities effectively. Sponsorship / work rights for Australia You must have unrestricted
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of relevant training and experience proven Computer Literacy in (Excel, Clampex/Clampfit, GraphPad Prism) proven research publication in relevant field strong track record of peer-reviewed publications in