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For certain study designs and sponsor types, Curebase can lead projects start to finish. We have unique experience in biotech, pharma, digital therapeutics, diagnostics, medtech products, interventional, observational data, and large-scale biospecimen collection studies.
You are the experts in the science. We’ve built world class best practices in patient and user experience. Combining the two on your protocol we help to enhance your study design for optimal recruitment, retention, and patient satisfaction. We handle all IRB submission both central and intstitutional.
Our network consists of over 300 health care providers. We have experience with over 50 Principal Investigators of all backgrounds and experience levels. Couple this with our in house staff of clinical research coordinators, and conduct powerful studies that reach patients at academics, community PCPs, mobile providers, and many more.
We want our customers and users to have access to expertise on our software. Work with us to configure our platform the way you want for best in-class user experience workflow. Our team will also train your staff, sites, and other users on how to use our software. The process is easy to start and quick to complete.
Make the most our of our seamless recruitment workflow by having us design and manage your recruitment campaigns. Our team works on building study brands, landing pages, and using digital and site based marketing to fully enroll your study.
We advise study teams and build patient communication plans that leverage a combination of automated and personal touch engagement techniques. Our SMS/email notifications and updates in addition to CRC outreach and support are available.
Project management should be easy and transparent. On each study our PMs build living timelines, provide access to real-time dashboards, and access to monitoring resources on studies. Leverage all or some of our traditional clinical operations functions to fully manage and monitor your study.
You are the experts in the science. We’ve built world class best practices in patient and user experience. Combining the two on your protocol we help to enhance your study design for optimial recruitment, retention, and patient satisfaction. We handle all IRB submission both central and instiutional.
Our network consists of over 300 health care providers. We have experience with over 50 Principal Investigators of all backgrounds and experience levels. Couple this with our in house staff of clinical research coordinators, and conduct powerful studies that reach patients at academics, community PCPs, mobile providers, and many more.
We want our customers and users to have access to expertise on our software. Work with us to configure our platform the way you want for best in-class user experience workflow. Our team will also train your staff, sites, and other users on how use our software. The process is easy to start and quick to complete.
Make the most our of our seamless recruitment workflow by having us design and manage your recruitment campaigns. Our team works on building study brands, landing pages, and using digital and site based marketing to fully enroll your study.
We advise study teams and build patient communication plans that leverage a combination of automated and personal touch engagement techniques. Our SMS/email notifications and updates in addition to CRC outreach and support are available.
Project management should be easy and transparent. On each study our PMs build living timelines, provide access to real-time dashboards, and access to monitoring resources on studies. Leverage all or some of our traditional clinical operations functions to fully manage and monitor your study.
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Meet with our team to discuss your protocol, and walk through ways we can execute your study.
Press Release
October 19, 2021
Publication
March 31, 2022
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