Clinical Trials Administrator (Start-Up Associate) …, Sunshine Coast Regional

UniSC Clinical Trials | Health HubMorayfield Level 5, $82,843
- $93,358 p.a., plus up to 17% employer superannuation Full-time (36.25 hours per week), 2 year fixed-term appointment The Opportunity UniSC has established a world‑class Clinical Trials operation that is strengthening the region’s clinical research capability and delivering innovative, regionally relevant research in collaboration with healthcare professionals, pharmaceutical leaders and key industry stakeholders. As a Start‑Up Associate, you will play a key role in supporting the successful delivery of clinical trial projects across the UniSC Clinical Trials network by providing high‑level administrative and specialist support in the preparation, coordination and submission of start‑up, regulatory and essential site documentation, ensuring projects are managed efficiently, compliantly and to the highest standard. You will
- Support the Regulatory and Start Up team to ensure all projects across the UniSC CT network achieve smooth transition from feasibility to recruitment within established timelines and quality standards.
- Support the Regulatory and Start Up team in the ongoing management of study documentation and communication with/handover to the clinical team.
- Provide administrative support to the Regulatory and Start Up Manager to assist in the overall management and compliance of regulatory and start‑up processes of the UniSC CT site network. About you You possess a robust understanding of the privacy principles governing health information and are committed to maintaining the highest standards of compliance, accuracy and confidentiality in all aspects of your work. Comfortable working both independently and within multidisciplinary teams, you bring a proactive and collaborative approach, using your initiative to drive tasks forward while contributing positively to shared project outcomes. Your ability to balance autonomy with teamwork enables the efficient management of clinical trial documentation, regulatory processes and competing priorities in a fast‑paced research environment. You will possess
- Completion of a relevant degree, with relevant experience or an equivalent combination of experience and qualifications.
- Sound knowledge of ICH Good 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. 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. For additional support during the application process, contact unisc‑ or call +61 7 5430 2830. Apply on Kit Job: kitjobau.com/job/3r3rvn