The Northern Clinical School
ResearchAssistant
“Research Assistant at The Northern Clinical School. Skills: research process facilitation, clinical trial coordination, basic science research support, data management, grant application support. facilitating the research process by assisting in the coordination and execution of routine research activities. support the preliminary stages of grant applications”
What You'll Achieve.
maintain research data integrity; ensure efficient communication with survey participants; maintain organised research records, readying data for presentations and reports; ensure data accuracy, integrity, and confidentiality
Industry & Context.
unrestricted work rights in Australia, willingness to work in a patient facing clinical environment, pre-employment or background checks
What They're Looking For.
Must Have
relevant tertiary qualifications or an equivalent combination of relevant training and experience, coordinating and/or managing grant application process, experience in managing, reporting, and disseminating research data, experiencing with diary management, project management, experience working on research projects with clinicians, experience working in hospital setting, willingness to work in a patient facing clinical environment, experience working with electronic medical records, Kiteworks and Redcap, excellent understanding of human ethics and governance process, completion of GCT/CTMS training, unrestricted work rights in Australia
Nice to Have
laboratory based experience, animal work experience
What You'll Do.
facilitating the research process by assisting in the coordination and execution of routine research activities
support the preliminary stages of grant applications
maintain research data integrity
ensure efficient communication with survey participants
contribute to maintaining organised research records
readying data for presentations and reports
support the coordination and delivery of clinical trial activities
including participant screening
conduct of study visits alongside clinicians
multisite coordination
and meeting administration
including minute-taking and follow-up actions
assist with the preparation
and ongoing management of ethics and governance documentation
support basic science research activities
including routine laboratory tasks
experimental procedures
and maintenance of accurate laboratory records under supervision
support the preparation of research reports
and other project-related documentation
maintain compliance with research protocols
regulatory requirements
including the preparation and maintenance of study documentation and logs
support data collection
and secure record management to ensure data accuracy
assist researchers with preliminary grant application activities
including collating supporting data and documentation
undertake additional research
and administrative duties appropriate to the classification level as required
How You'll Work.
Team & Collaboration
working on research projects with clinicians; conduct of study visits alongside clinicians
Communication Scope
efficient communication with survey participants
Process & Methodology
diary management, project management, multisite coordination, coordination and delivery of clinical trial activities
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