We are experienced in the conduct of successful, safe, and on-budget delivery of clinical trials including the implementation of clinical trial protocols, data management, grant applications, and ethics submissions. 

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We provide central coordination for multi-site trials, as well as site-specific support from study initiation through to study closure, including safety and data monitoring. We work with the protocol investigator team to operationalise the trials and we work with sites on the development and improvement of participant recruitment strategies.

We also provide education and training, biostatistical and health economics expertise, and an array of data management services including case report form development, database setup, data collection, and data entry support. Using a risk-based program we conduct monitoring to ensure rigorous reliable trial data capture within the principles of Good Clinical Practice.

Our skilled writers help you to develop clinical trial protocols, generate literature reviews as well as prepare grant applications and ethics submissions.

We have a strong track record of supporting investigator-initiated clinical trials. We also welcome collaborations with industry.

Contact us to discuss your study idea.