Clinical Trials Coordinator (Caboolture)

UniSC Clinical Trials Coordinator – Health Hub Morayfield, Sunshine Coast Level 6, $95,986
- $103,873 p.a., plus up to 17% employer superannuation; Full-time (unspecified hours), 2‑year fixed‑term appointment. The Opportunity As a Clinical Trials Coordinator, you'll be at the heart of delivering high‑quality, compliant clinical trials that contribute to better health outcomes. Responsibilities
- Contribute to the coordination and administration of designated clinical trials within UniSC CT.
- Work collaboratively with the CTC team, sponsors, and monitors to ensure the successful conduct and timely completion of clinical trials. NOTE: This role requires flexibility to travel to different clinical trial sites, to work outside standard business hours to support confinement studies and other time‑sensitive trial activities. You may also be required to participate in a 24/7 on‑call or confinement roster. About you Organised, proactive, and always thinking ahead, you bring calm confidence to the fast‑paced world of clinical trials. With a steady hand and sharp eye for detail, you're comfortable juggling multiple studies, keeping protocols on track, records accurate, and stakeholders informed. You're curious and composed, ready to solve problems, guide participants with care, and support the team with everything from ethics submissions to continuous process improvement. You understand the big picture but never miss the fine print. Whether you're working with clinicians, engaging with participants, or collaborating across teams, you know how to keep the process moving forward, smoothly and successfully. Qualifications
- Completion of a degree qualification in Health, Science, Nursing, or related field with subsequent relevant experience or an equivalent combination of experience and Diploma qualification.
- Registered Nurses must have current registration with AHPRA; Enrolled Nurses must be medication administration endorsed and have phlebotomy training and experience.
- Knowledge of ICH, Valuable Clinical Practice, and applicable regulations.
- High‑level computing skills (including databases, clinical trial electronic data entry, word processing and spreadsheets).
- Sound understanding of privacy principles governing health information.
- Ability to work independently and as part of a multidisciplinary team.
- Previous Clinical Trial Coordination experience highly regarded. Benefits
- Up-to-date teaching & research facilities.
- Professional development and career pathway opportunities.
- Recipient of the Athena SWAN Bronze Award.
- Flexible work arrangements & generous leave options.
- Salary packaging options + 17% super.
- EAP, fitness passport & discounted private health. UniSC is an equal opportunity employer, committed to diversity and inclusion. We encourage applications from all backgrounds, including those with disabilities, women in STEM, First Nations Peoples, and individuals of diverse cultures, genders, abilities, and experiences. We value achievement relative to opportunity and encourage your commentary on your achievements in this context. #J-18808-Ljbffr Apply on Kit Job: kitjobau.com/job/3rv7sr