At Paratus Clinical, we’re committed to running research that is not only scientifically strong, but also participant-focused, respectful, and accessible.
That’s why we’re creating an advisory panel, a small group of community members who have been invited to share feedback and help improve how our studies are designed and delivered.
The advisory panel is a team of 5 participants who work alongside our doctors and clinical trial staff to provide input on the participant experience.
About the panel
A team of invited participants who work alongside our doctors and clinical trial staff to provide input on the participant experience.
What the panel does
Board members may be asked to review materials, comment on communication, and identify practical barriers that could affect study completion and retention.
Participant information sheets and consent forms
Clinic visit schedules and time commitments
Communication materials including emails, SMS reminders, brochures and website information
Recruitment messaging and participant support
Overall participant experience and what could be improved
Trial suitability and potential barriers for completion and retention
This opportunity is for people who have been invited and enrolled into the Paratus Exclusives Program.
You do not need any medical or research background. We’re looking for people willing to share honest perspectives and help make trials better for others.
To ensure fresh perspectives, the advisory panel rotates regularly. The panel has 5 members in total, each term runs for 3 months, and positions may open four times per year.
If selected, our team will contact you with next steps. You may be invited to join a short online session, review participant-facing materials, or provide written feedback by email.
Your feedback helps us understand what participants need before, during and after a clinical trial. By sharing your perspective, you can help make study information clearer, visits easier to manage, and the overall experience more supportive.
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Paratus Clinical is proud to be a Society for Clinical Research Sites member. We actively participate in discussions and decisions that ultimately impact the industry at large. Being a part of the SCRS community gives us the opportunity to be heard and allows us to partake in industry training and events.
T: 1300 742 326
