We employ clinical research staff that work at our affiliated urology practices in partnership with our physicians to conduct studies and enroll patients.
Study Sourcing
We leverage our network of sponsors to identify studies that could be a good fit for each of our sites.
Contracts and Budgeting
We negotiate a master clinical trial agreement (CTA) and study budget with sponsors on behalf of our affiliated practices.
Regulatory and Compliance
We manage all regulatory files and IRB submissions. We also oversee compliance and handle monitoring visits with sponsors and CROs over the course of the study.
Equipment Sourcing
We help source equipment needed for new partner sites to prepare for upcoming studies and coordinate calibration.
Data Entry
We manage data entry and use a clinical trial management system (CTMS) that keeps track of all patient visits and serves as a repository for all study documents.
Recruitment
We assist sites with patient recruitment through a variety of strategies.
Finance
We prepare and send out invoices for visits completed, interacting with sponsors to collect any funds earned over the course of the study.
Standard Operating Procedures
We utilize standardized SOPs across our network to ensure a consistent level of quality is met at all sites.
