Studybox Research Site solutions · Urgent care & medical practices
Earn Revenue with Research.
Participate in low-effort diagnostic studies with seamless integration into your existing workflow. We handle the research, you see the patients.
For Clinics
Site solutions · Urgent care & medical practices
Why partner with us
Boost Income & Scale Operations.
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Revenue Generation
Clinics and patients earn additional income from research participation, supporting clinic operations and quality care.
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Seamless Integration
We place experienced coordinators in clinics to manage research studies, including patient recruitment and compliance while using the site staff to collect, test and interpret the investigational product.
What makes us different
We Don't Do Drugs.
Unlike therapeutic drug studies, In-Vitro Diagnostic trials involve no investigational treatments, no follow-up visits, and no added patient risk. Participation fits within standard clinical care: a patient presents with symptoms, a specimen is collected, and the investigational device is tested alongside existing workflow.
Inside a study visit
How It Works.
One visit
6
steps, start to finish
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Patient arrives presenting with signs & symptoms consistent with the indication of study interest.
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Clinic staff identifies potentially eligible patients in the course of routine patient care.
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Clinic staff notifies Studybox Coordinator of eligible patient.
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Coordinator explains the study and enrolls patient via informed consent.
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Clinic staff collects required specimen(s), tests on device, and interprets results.
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Studybox Coordinator releases subject and provides payment.
FAQ
What Practices Ask Us.
01 How much staff time is required?
Very minimal. Our coordinator handles all study-related tasks. Existing staff only collect the specimen and test the device, exactly what they do in standard care.
02 Do patients need to return for follow-up visits?
No, generally studies only require a single visit. There are no investigational treatments, no medications, and no follow-up required. The patient's experience is indistinguishable from a routine visit.
03 What are the compliance and regulatory requirements?
We take on the administrative heavy lifting: regulatory submissions, IRB approval coordination, and documentation. Site staff and your PI retain responsibility for study conduct, so we provide hands-on training to make that easy, keeping your day-to-day close to standard care while ensuring everything stays compliant.
See if your practice qualifies
Submit & Qualify Your Practice.
Become a clinical research site: tell us about your practice and Talia will reach out within one business day. Questions first? Contact us.
Practice qualification cardNo postage necessary