UC

UniSC Clinical Trials

Verified Job Source

Breakthrough medical treatments and therapies that help people live well and live longer are on our horizon.

Sippy Downs, Queensland

Research Services
51–200 people

About

UniSC Clinical Trials is a growing clinical trials network that partners with healthcare professionals across the Sunshine Coast, Moreton Bay and Brisbane regions, and beyond.​ We work with local and global medical experts and industry to bring advanced treatments and therapies to life, and make cutting-edge medical research accessible to everyone.​ We aim to meet needs and demand for new interventions as we make medical breakthroughs across an ever-expanding portfolio of therapeutic areas, addressing a wide range of diseases and conditions.​ Our facilities integrate research, and the development of new medical innovations with healthcare delivery, ensuring that the community benefits from the latest advancements in medicine.​ But our true point of difference is our people-first approach and commitment to community.​ We combine priority with passion to create safe and positive patient experiences, to ensure quality outcomes for everyone.

Open positions

Senior Clinical Trial Coordinator

On-site · Sunshine Coast Regional District

You will lead clinical trial teams to ensure all research is conducted according to ICH/GCP standards and internal SOPs. The role involves managing complex trial activities, collaborating with sponsors, and participating in a 24/7 on-call or confinement roster.

Clinical Trials Contracts Administrator

On-site · Sunshine Coast Regional District

The administrator will manage the review, negotiation, and finalization of clinical trial agreements while providing governance support. They will also coordinate with internal teams and external partners to ensure compliance and efficient project execution.

Clinical Trials Coordinator

On-site · Sunshine Coast Regional District

The Clinical Trials Coordinator will lead assigned studies by managing patient visits, data collection, and regulatory compliance according to ICH/GCP guidelines. They will also coordinate study start-up, ethics submissions, and collaborate with multidisciplinary teams to ensure effective trial delivery.