Quality. Results. Reputation.
Are you searching for an experienced research site for your clinical trial?
Choose the one who has it all — JBR Clinical Research.
Leading the acute analgesic research industry for over three decades.
We are selective in both who we work with and the types of studies we engage in. We are careful not to overstate our ability and quick to provide accurate projections for what we can accomplish. With this mentality and transparency, JBR has stayed true in becoming and staying number one in our field of expertise.
JBR Clinical Research is the premier dental pain study site in the world.
JBR is one of the top hard and soft tissue analgesic research sites in the U.S.
JBR trains staff via pilot studies and analgesic methodology training.
JBR retains board-certified on-staff physicians and mid-level providers.
JBR has access to a healthy patient population in and around Salt Lake City, UT.
JBR has a database of over 80,000 to make enrolling fast and cost-effective.
JBR maintains an in-house, full-time recruiting team to qualify volunteers.
JBR retains a full-service ad agency for study outreach and community education.
JBR retains contract with protocol development expert Stephen Cooper, DMD PhD.
JBR retains contract with leading methodology expert Georgia Simmons RN, BSN, CCRP.
Our dedication to training is second to none.
We invest more time and money to conduct pilot study training than any other research site in the country. Our staff is methodology trained with didactic presentation and hands-on pilot study training to ensure our study coordinators can separate from placebo. This focus on training our people is what gives us the competitive advantage in the marketplace and ultimately provides the quality data that your research projects demand.
We’ve fine-tuned our marketing and recruiting teams to give you access to a large population of healthy volunteers, with over 80,000 patients in our database.
Clinical expertise. Strategic focus.
JBR Clinical Research has conducted hundreds of studies, and our long-time staff has benefitted from the variety, complexity and volume of our clinical research engagements. Our average tenure among key personnel is over 10 years. We consult with our sponsor and CRO partners in protocol development, analgesic project planning, and all aspects of Phase I through IV clinical trials. The importance of a dependable, easy-to-work-with site is paramount, and we deliver results.