Welcome
About us
Cura Clinical Research is the result of 25 years of research experience and over 200 studies conducted. We have experienced staff and enough staff to cover any needs the clinical trial may need as well as any equipment that is required.
BENEFITS
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Cura is able to perform labs onsite.
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Cura works directly with the Central IRB.
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There are no additional committees for review.
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Can complete IRB and contract/budget in parallel with one another.
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Start-up process can be completed within 2 weeks.
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Only have to deal with one contract/budget team for all sites.
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Cura offers great monitoring accommodations, with availability Monday to Friday 9am-5pm.
STATISTICS
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Cura has a 90% Retention Rate
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There is a low Screen Fail Rate of 10%
PI AVAILABILITY AND INVOLVEMENT
The PI is always available to answer any questions and is available as needed. The PI is hands on, and sees the subjects at each required visit. The PI will complete the required scales, and review all labs and EKG’s within a 24hr period. The PI is part of the ICF process, inclusion/exclusion criteria, any AE/SAEs and is knowledgeable about what is occurring at each subject visit.