A proven Phase I–IV site network built for rapid, high-quality enrollment.
Prime Research Institute delivers end-to-end trial management across three dedicated research sites — from first-in-human dosing to large pivotal programs.
Purpose-built for complex protocols.
Our flagship site supports early-phase, intensive monitoring, and long-term inpatient stays — with redundant safeguards for every specimen and dose.
Facility amenities
- Three exam/procedure rooms
- Early Phase/Phase 1 in-patient unit (3 beds)
- Flat screen TVs for overnight and in-patient stays
- Catered meals for in-patient stays
- Locked and secured archive room for document storage
- Fully equipped lab and phlebotomy room
- Access to washer/dryer and laundry facilities
- Monitor offices with copier/fax/scanner and supplies
- WiFi available throughout the facility
- Conference/meeting room
- Private work room
- Secured and alarmed facility
- 24/7 video monitoring of general areas
Medical & diagnostic equipment
- EKG machines (12-lead) on-site (2)
- YSI Stat Plus 2300 glucose analyzers (1)
- Laminar flow hood
- Calibrated blood pressure monitors and weight scales
- Emergency crash cart, oxygen tank, and defibrillator
- FibroScan
- Infusion pumps (3)
Drug & specimen storage
- Back-up generator system
- 24/7 temperature monitoring alarms for all drug & lab refrigerators and freezers
- Refrigerated centrifuges (1)
- Micro centrifuges (1)
- -70°C freezers with 24/7 alarmed temperature monitoring (1)
- -20°C freezers with 24/7 alarmed temperature monitoring (1)
- Scientific-grade refrigerator for drug storage with 24/7 alarmed monitoring and backup generator
- Ambient drug storage room with 24/7 alarmed temperature monitoring
- Controlled substance double-locked and alarmed cabinet
- Hazardous shipping certified clinic and lab staff
From protocol to enrollment, in four steps.
A streamlined sponsor experience designed to shorten startup and keep enrollment on schedule.
Submit a study
Share your protocol, IB, and enrollment targets through our sponsor intake — we respond within 48 hours.
Feasibility & budget
Our medical team completes a documented feasibility review and delivers a transparent budget and CDA.
Rapid activation
IRB submission, contracts, and site activation handled in parallel to compress startup timelines.
Dedicated enrollment
A named coordinator team drives recruitment from our 12,000+ participant database across three sites.
Ready to activate your trial?
Contact our business development team to discuss feasibility, capacity, and timelines.
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