-
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
-
governance processes, including ethics submissions, amendments, trial registration, and compliance with data governance and institutional requirements · contribute clinical insight, drawing on intensive
-
· 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
-
‑resilient health systems · manage research ethics and governance processes, including trial registration, ethics submissions, amendments, and compliance reporting · contribute to national and
-
that enhances policy, practice, industry, and community outcomes · work effectively with multidisciplinary teams including clinicians, human factors experts, computer scientists, and AI experts
-
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
-
manuscripts and conference presentations contribute to competitive research grant applications, ethics submissions, governance processes and reporting requirements coordinate and manage project timelines, team
-
groups, and build effective relationships across organisations with diverse needs and priorities demonstrated capacity to coordinate all aspects of the research process including study design, ethics
-
design, ensuring quality, transparency, and excellence in all research activities · oversee ethics and governance processes, including trial registration, ethics submissions, amendments, and ongoing
-
. 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