Why CHOOSE OUR SMO ? 

By choosing to partner with Clinitrials, you will have access to quality research sites well equipped to meet study targets and deliver successful trial outcomes. Our model allows us to work with multiple Investigators and affiliated referral centers to improve access to clinical trials and increase trial participation.

Our experienced clinical research staff 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 over 750 participants and has allowed us to successfully complete many clinical trials. 

Centralised Activities

• Feasibility and site selection

• Study start up activities from site selection to SIV

• Budget and Contracts negotiations

• Protocol implementation plans

• Recruitment plans and activities to achieve recruitment targets

• Study documentation templates including source worksheets

• Trial administration during the study including HREC and Governance submissions

• Risk assessment and Quality Management system

 Quality Management System

• Principal Investigator oversight processes

• Standard Operating Procedures

• Risk and Issue Management

• Metrics and Objectives

• Vendor Partnering

• Internal audits

• Training, education and delegation

Participants are at the centre of what we do. Planning and activities, revolve around participant involvement and safety. This results in high quality data, improved enrolment and increased retention.

To learn more about our sites click on the link above.

To enquire if we can assist with the success of your research study , please email us at info@clinitrials.com.au