OUR CAPABILITIES  

By choosing to partner with Clinitrials, you will have access to quality research site(s) 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 Capabilities

• Efficient and timely study start up

• Experience in a diverse range of therapeutic areas

• Provide quality outcomes

• Early focus on recruitment

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 1000 participants and has allowed us to successfully complete many clinical trials. 

Centralised Activities include

• Feasibility and site selection

• Study start up activities from site selection to SIV

• Budget and Contracts negotiations

• Protocol implementation plans

• Recruitment strategy to help meet recruitment targets

• Study documentation templates including source worksheets

• Trial administration during the study including HREC and Governance submissions

• Quality Management system

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