McAllen Research Delivers
Confidence in Clinical Trials

Sponsors and contract research organizations (CROs) around the world partner with McAllen Research to
support clinical studies for drugs, medical devices, diagnostics, and combination products.

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Diverse Experienced Investigators
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Clinical trials conducted since 2019
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Patients Enrolled

Whether you’re ready to conduct a single-site study or a complex, high-volume clinical trial, trust Velocity to deliver the right investigators, clinical staff, and patients.

Designed for the Next Generation of Human Health Research

Led by experienced investigators and research teams, McAllen Research is built to deliver high-quality results, reliable performance, and exceptional efficiency—even for the most complex clinical trials.

Full Alignment

Seamless Site Management

Fast and seamless site selection and contracting processes to get your study started quickly.

Fast Activation

Rapid Study Activation

Streamlined study start-up with centralized initiation activities and digitized source, regulatory, and records management.

Reliable Enrollment

Exceptional Patient Engagement

Expert patient engagement teams drive top-tier enrollment and retention programs for every study.

High Quality

High-Quality Oversight

Comprehensive in-house quality and data management, with rigorous monitoring and oversight powered by a unified technology system.

Full Alignment

Fully Integrated Operations for Faster Site Selection

At McAllen Research, our operations are designed to maximize the quality and efficiency of clinical trials. From the very start, we help you accelerate site selection with fast, accurate responses to site questionnaires.

Your trial management team enjoys the same benefits throughout the study: centralized communication, standardized site processes, and industry-leading oversight.

Many of McAllen Research’s investigators and leaders are also consulted on protocol design, providing insights that strengthen the feasibility and success of research programs. Combined with our centralized approach, their expertise ensures more predictable and efficient trial performance.

  • Phase II-IV capabilities
  • 3600 sqft office with 14 rooms
  • Secure WIFI
  • Dedicated Conference Room
  • Dedicated Monitoring Room
  • Secure Investigational Products Storage
  • Secure Laboratory and Storage
  • Calibrated Vital Signs Equipment
  • In-House Fibroscan
  • Ambient/Refrigerated Centrifuge
  • -20 Pharmacy-grade Freezer
  • -80 Freezer
  • AED/ ACLS-Crash Cart
  • Back-up Generator
  • 24hr continuous temperature monitoring with alarm (iMonnit)
Fast Activation

Fully integrated operations to support rapid site selection

McAllen Research goes beyond the traditional site network or SMO model. By applying a systematic approach to site setup and oversight, we can quickly initiate studies while maintaining operational excellence—even for complex trials. With digitized source documentation, regulatory management, and records tracking, McAllen Research can efficiently start, scale, and optimize your study operations.

In addition to supporting the essential infrastructure, we can integrate new technologies or treatment approaches to run specialized, decentralized, or hybrid trials.

• Clinical Trial Management System

• Secure WiFi

• eConsent capability

• eRegulatory available

• Expereinced staff in ePRO and eCOA systems

Reliable Enrollment

Expert Patient Engagement and Retention Solutions

McAllen Research is designed to meet and exceed enrollment and retention goals, even for high-volume or hard-to-recruit studies. With a dedicated technology team and fully managed Patient Engagement and Recruitment Centers, we continuously optimize recruitment, screening, consenting, retention, and follow-up processes to benefit both clients and participants.

Every McAllen Research site is supported by full-time recruitment specialists to drive local outreach. Sites are strategically located in demographically diverse areas to ensure proportional representation in clinical trials.

  • Access to proprietary physician and practice databases

  • Immediate enrollment support from study initiation

  • Targeted community outreach and diversity-focused initiatives

  • In-house advertising solutions that outperform centralized campaigns

  • Participant adherence and retention programs

  • Specialty care sites providing access to niche populations, procedures, and facilities

High Quality

Fully integrated operations to support rapid site selection

McAllen Research delivers industry-leading quality oversight with in-house clinical data, QA, regulatory, and risk management teams supporting every site and study.

Our experienced teams work alongside site staff to identify opportunities for continuous improvement, ensuring adherence to FDA regulations, ICH GCP guidelines, state rules, industry standards, and McAllen Research’s rigorous SOPs.

  • 48-hour data entry and query resolution

  • Routine and random QA reviews with EDC/source cross-checks

  • Continuous investigator and site staff training

  • CLIA-certified labs, IATA-certified staff, GCP-trained physicians and personnel

Explore more at McAllen Research

Let’s talk about your next trial

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