The Nurses at Dedicated Clinical Research Coordinators understand enrolment and retention of participants to a clinical trial is essential to achieving the approval of new treatments for all.

We work closely with the site patient recruitment platform to facilitate wide community involvement and centralised management of recruitment progress via a central portal.

For best results, site staff focus on study visits while our Nurses conduct pre-screening of large numbers of patient enquiry, forwarding onto site only those who fit the criteria and are available for study visits.

Protocol specific information such as rationale, duration, and location of the trial and the importance of clinical research globally is discussed as well as confidentiality and of particular importance, the Informed Consent process.

This “patient centric” approach demonstrates respect for participants and compliance with principles of ICHGCP.

Get in touch and let’s work together to achieve patient recruitment for your trial.

Site management is essential for the successful completion of any clinical trial. Due to site variances, so does the plan for success. Our team prefers to engage early in the process where possible and seeks to understand the demands of the Protocol, and existing site structure to highlight potential pain points.

Our team propose tailored solutions in addition to compliment the existing team with identified issues. Together we make the process happen, while ensuring clear expectations and responsibility frameworks.

Through experience and qualifications, our team anticipates and prevents issues, being solution focused.

Our team can expand capacity fulfilling blinded and unblinded roles by providing;

• Clinical research infrastructure

• Establishing systems and trackers to ensure protocol compliance

• Qualified support to relieve team illness or leave requests

• Manage investigational product and equipment eg. temperature regulated fridges

• Addition support through remote patient recruitment, in person patient visits on site, assessment per protocol and all aspects of the administrative burden

With 18 years experience in Pharmaceutical and Medical Device trials, Louretta offers as-needs specialist supports. Areas that Louretta provides practical solutions in include;

• Human Research Ethics Committee (HREC) submissions

• Site selection

• Staff training

• Innovation through a problem solution framework