FOR SPONSORS & CROS

A research partner.
Rooted in El Paso.

Independent research operations within a physician-practice setting. Review the people, access, facility resources, and workflows that may fit your protocol.

The El Paso Clinical Trials location
El Paso, Texas · Outpatient research site

Site snapshot.

The essentials for an initial feasibility review. Protocol-specific investigator availability, qualifications, equipment, and timelines are confirmed directly.

01

Site model

Independent, community-based, and physician-connected in El Paso, Texas.

02

Investigator network

Verified specialties spanning family and sports medicine, psychiatry, ophthalmology, rheumatology, radiology, internal medicine and pathology, orthopedic surgery, and pain/anesthesiology.

03

Participant access

Physician-practice access, regional referrals, community outreach, digital recruitment, and English/Spanish follow-up.

04

Facility & equipment

Private consultation and examination areas, ECG, vital signs, phlebotomy, refrigerated centrifugation, cold storage, controlled investigational-product storage, and monitor workspace.

05

Study operations

Feasibility, startup support, visit coordination, source and regulatory workflows, sponsor-required data entry, query follow-up, and monitoring support.

06

Protocol fit

Indication, study phase, eligibility profile, visit schedule, staffing, equipment, and timelines are reviewed case by case.

Therapeutic fit, without guesswork.

These areas reflect verified investigator specialties and relevant site experience. They are capabilities to discuss—not a list of studies currently recruiting.

Musculoskeletal, osteoarthritis & pain

Family and sports medicine leadership with orthopedic, rheumatology, and pain/anesthesiology collaboration.

Behavioral health & addiction

Psychiatry expertise that includes general, addiction, and child and adolescent psychiatry, together with prior opioid use disorder research experience.

Rheumatology & inflammatory conditions

Protocol-specific rheumatology investigator collaboration and outpatient research operations.

Ophthalmology

Protocol-specific ophthalmology investigator collaboration supported by EPCT research coordination.

Investigator participation and delegated responsibilities are confirmed for each protocol.

From feasibility to follow-up.

01

Protocol & investigator fit

Review the indication, study phase, eligibility profile, visit schedule, staffing, equipment, and timeline with research leadership.

Meet the investigator network
02

Patient access & recruitment

Physician-practice access, regional referrals, community relationships, and digital outreach support study-specific recruitment conversations. English and Spanish communication supports follow-up.

03

Study coordination & data

Coordinate visits, source documentation, sponsor-required data entry, and query follow-up under investigator oversight and protocol-specific delegation.

04

Start-up & monitoring

Discuss essential records, study-system access, training, monitoring arrangements, and the requirements for your protocol.

Clinical space. Practical resources.

Participant visits

Private consultation and assessment areas, examination rooms, ECG, vital signs, phlebotomy, and protocol-trained procedure support.

Specimens & investigational product

Refrigerated centrifugation, refrigeration and freezer capacity, temperature-controlled investigational-product storage, and restricted-access supplies. Confirm protocol-specific requirements and qualification records during feasibility.

Monitoring & documentation

Dedicated monitor and conference workspace, wireless access, print/scan support, and controlled access to electronic source and regulatory records. Paper source can be maintained when a study requires it.

Examination rooms at El Paso Clinical Trials
Authentic EPCT examination spaces

The Borderland is part of the study context.

Local understanding matters in recruitment and retention.

El Paso serves a substantial Hispanic/Latino community at the U.S.–Mexico border. Our site connects study conversations with local physician relationships, bilingual participant support, and community outreach.

We assess the recruitment plan for each protocol rather than assuming that a regional population number translates into eligible participants.

Our community approach

Start a useful feasibility conversation.

Share your organization, therapeutic area, study phase, anticipated timeline, and the site requirements you want to discuss. We can arrange the appropriate exchange of protocol documents and qualification materials.

Abraham Arzola, BS · Director of Research

Please do not send participant information in an initial website inquiry.