Why partner with our sites?
By choosing to partner with Clinitrials, you will have access to quality research sites with experienced and dedicated clinical research staff. By incorporating our stringent quality management processes, our sites are well equipped to meet study targets and deliver successful trial outcomes.
The staff at Clinitrials have worked as either Study Co-coordinators, Research Nurses, Research Assistants, Project and/or Trial Managers - and nearly every position in between - and have a thorough understanding of the issues involved in running a successful clinical trial at site level.
You can be confident we have the capabilities and experience to conduct your trial. Our reputation for excellence is built upon the contributions of many participants and has allowed us to successfully complete many clinical trials.
Centralised Activities
HREC submission - designated start up specialist
Budget and Contracts negotiations
Source documents ( ALCOA C )
Training
Trial administration
Internal QA – some of our staff are also monitors/ CRA’s so we conduct internal monitoring
Staff and Facilities
Experienced study staff
All staff have current (within 2 years) GCP training certificates
Staff have experience with a range of eCRF systems and study portals
Quality Management Processes
Principal Investigator oversight processes in place
Standard Operating Procedures
Internal Quality Assurance program
GCP compliant Source Document template
Equipment compliance program
Training and education
To learn more about our capabilities ....click here
Our research sites
