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Prepare examples of protocol adherence, eligibility screening judgment, adverse-event documentation, and clear participant communication under ethics and reporting rules.
Best suited to organized, detail-focused coordinators who can manage people and paperwork in regulated research at Griffith’s Gold Coast campus.
As a Clinical Trial Coordinator at Griffith University, you would schedule study visits, screen eligibility, run protocol measures such as interviews or vitals, prepare ethics and progress documentation, brief participants, and record adverse events with investigators for university-hosted trials.
Strengthen health-science fundamentals with:
No. The listing is for Southport, Gold Coast, with remote set to on-site.
Scheduling subjects, screening eligibility, protocol procedures, study documentation, and adverse-event reporting.
Saylor Academy Health Sciences courses are free; Coursera healthcare courses are free to learn on the audit track.
Public-domain labor data — prepare examples for 2–3 of these.
Website: griffith.edu.au
Griffith University is a public research university in South East Queensland on the east coast of Australia. The university was founded in 1971, but was not officially opened until 1975. The university has five campuses, at Gold Coast, Nathan, Logan, South Bank, and Mount Gravatt. A sixth campus, to be located at the Treasury Building in the Brisbane CBD, will open in 2027. The university was named after Sir Samuel Walker Griffith, who was twice Premier of Queensland and the first Chief Justice of the High Court of Australia. Sir Samuel Griffith played a major role in the F…
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Clinical Trial Coordinator at Griffith University, Southport, Gold Coast About This Position The role of a Clinical Trial Coordinator at Griffith University involves managing day-to-day operations for one or more clinical trials in Multiple Sclerosis (MS) at the university's Clinical Trial Unit on the Gold Coast campus. You will be responsible for coordinating all aspects of trial delivery, from screening and enrolment through to completion. Core Duties Manage day-to-day operations of clinical trials in MS Coordinate all aspects of trial delivery including scheduling, data collection, and documentation Ensure compliance with regulatory requirements and institutional policies Screen and enrol participants as per the study protocol Collaborate with multidisciplinary teams to ensure smooth trial operations Prepare and maintain accurate records for each trial Qualifications Degree in a relevant field such as nursing, medical science, or health sciences Experience in clinical research or related field preferred Familiarity with MS and its treatment options is beneficial Strong organizational skills and attention to detail Excellent communication and interpersonal skills Proficiency in Microsoft Office Suite and data management software Why Join Griffith University Griffith University offers a dynamic environment for research and innovation. As part of the team, you will have access to state-of-the-art facilities, collaborative opportunities with leading researchers, and a commitment to excellence in education and research. Ready to Apply? To apply, complete your application directly on this page, or you'll be redirected to the employer's application platform to finish submitting there. View full listing & apply (via Adzuna)
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