GP clinics and hospital departments with the right patient populations and clinical staff can participate in our research network, generating additional revenue while offering patients access to investigational treatments.
Participating sites receive per-patient fees for every enrolled participant, covering screening, visits, and study completion. All training, regulatory coordination, and sponsor-facing documentation is handled by our central team.
We start with a conversation about your practice, your patient population, and the therapeutic areas where you see the most opportunity. No commitment required at this stage.
We review your clinic's infrastructure, record systems, and staff capacity against specific trial requirements. We are honest about where you are ready and where preparation is needed.
Staff complete GCP training funded by AUC Trials. We provide SOPs, delegation logs, and all documentation frameworks. We do not leave sites to figure this out alone.
Once a suitable sponsor protocol is matched to your site, we manage regulatory submissions, site initiation, and ongoing monitoring. You focus on the patients.
We do not expect sites to build a research function from scratch. We bring the framework, the expertise, and the sponsor connections.
A complete set of GCP-compliant standard operating procedures covering all aspects of site conduct, tailored for community clinic settings.
All site staff involved in trial conduct receive GCP training funded by AUC Trials. Training records and refresher cycles are maintained centrally.
TGA CTN submissions, HREC applications, and institutional governance approvals are managed by our central regulatory team. Sites review and sign; we do the preparation.
We match qualified sites to appropriate sponsor protocols. You benefit from our existing sponsor and CRO relationships without having to build them independently.
A dedicated study coordinator from our team is assigned to each trial. They handle query resolution, data entry support, and communication with the sponsor monitor.
Sites receive per-patient fees and visit fees for each enrolled participant. Payment timelines are defined in the site agreement and tied to sponsor invoicing milestones.
Send us a brief overview of your practice and patient population, and we will schedule an initial conversation with no commitment required.