About Zentric
A new generation of clinical research, backed by deep experience
Zentric Clinical Research is a newly established, independent clinical research site on the Gold Coast, Queensland — backed by a leadership team with more than 20 years of clinical research experience.
- OUR FOUNDATION
Experience behind a new generation of clinical research
While Zentric is newly established, its leadership team brings more than 20 years of clinical research experience -spanning site management, study delivery, sponsor and CRO collaboration, and participant care. This combination allows Zentric to offer the responsiveness and agility of a new site, with the rigour, quality focus and operational maturity expected by pharmaceutical companies, biotechnology organisations and CROs. Zentric is positioned as an independent, purpose-built, investigator-focused and participant-focused and participant- focused research site-quality driven and research-ready.
Independent
We operate as a fully independent clinical research site, free from institutional constraints — enabling us to be responsive, flexible and focused on your study.
Purpose-built
Zentric was designed from the ground up for clinical research. Every process, facility and team member is aligned to delivering quality research outcomes.
Participant-focused
We believe the best research outcomes come from treating participants with genuine care, transparency and respect throughout every study.
Quality-driven
A strong commitment to quality, protocol compliance, participant safety and regulatory requirements underpins everything we do.
Our People
Experienced leadership team.
Our leadership team brings more than 20 years of clinical research experience across a broad range of therapeutic areas and study phases.
The Zentric leadership team brings over 20 years of combined clinical research experience, spanning Phase 1–4 studies across multiple therapeutic areas. Our team has a deep understanding of what sponsors, CROs and participants need from a research site.
Our commitments.
All studies are conducted in accordance with ICH Good Clinical Practice guidelines.
Participant welfare is our highest priority in every study we conduct.
Rigorous adherence to study protocols and sponsor requirements.
Full compliance with Australian regulatory requirements and TGA guidelines.
Robust data management processes to ensure accuracy and completeness.
All research conducted with full ethical oversight and HREC approval where required.