Why Partner With GLRI El Paso Research?
El Paso Research is a fully equipped, independent clinical research site with the infrastructure, equipment, and experienced personnel required to support Phase II–IV clinical trials. Our team is trained in the proper use, maintenance, and documentation of all study-related equipment to ensure data accuracy, participant safety, and protocol compliance.
On-Site Equipment
Our facility is equipped to support a wide range of metabolic, renal, and general medicine protocols, including studies requiring cardiac monitoring, biospecimen processing, and temperature-controlled storage.
Key Equipment Includes:
12-lead EKG machines
Ductless Fume Hood
-20℃ Fridge
-80℃ Fridge
Ambient Centrifuge
Refrigerated Centrifuge
All equipment is routinely maintained, calibrated as required, and monitored per SOPs and sponsor requirements.
Capabilities
Site staff are experienced in:
Proper operation and documentation of EKG procedures
Biospecimen processing, centrifugation, aliquoting, and storage
24/7 temperature monitoring and excursion management
Sample preparation for local and central laboratory shipments
Compliance with protocol-specific handling and timing requirements
Our team follows established SOPs and sponsor guidance to ensure consistency, accuracy, and audit readiness.
Therapeutic & Study Experience
GLRI El Paso Research conducts Phase II–IV clinical trials across multiple therapeutic areas, with specialized expertise in metabolic and related conditions.
Therapeutic Experience Includes:
- Obesity Studies
- Diabetes/Hypertension and metabolic disease
- Vaccines
- Kidney and renal-related research
- Gastrointestinal Studies
- General and chronic disease management
Experienced Investigators
Our site is led by experienced Principal Investigators with clinical and research backgrounds in:
- Family Medicine
- Nephrology
- Gastroenterology
This multidisciplinary investigator structure allows us to support a broad range of protocols while ensuring appropriate medical oversight and subject safety.
Accelerated Start-Up, Efficient Screening, and Consistent, Reliable Results
Our site prioritizes rapid start-up and efficient screening timelines in recognition of the fast-paced and competitive nature of metabolic studies. Our site delivers quick turnaround results while maintaining strict protocol compliance, participant safety, and high-quality data in alignment with sponsor and CRO requirements.
Quality & Compliance
- ICH-GCP and IATA–trained staff
- IRB-compliant processes
- Protocol adherence and safety oversight
- Capability to support both remote and on-site monitoring
- Audit-ready documentation and workflows
- Established and maintained Standard Operating Procedures (SOPs)
