Network Performance at a Glance
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Active & Completed Studies
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Average Site Startup Time
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Therapeutic Indications
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Minority Patient Enrollment
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Research Sites Across Texas
What We Bring to Your Study

Network Capabilities Built for Sponsor Confidence

Phase I–IV capabilities across multiple Texas sites — from first-in-human through post-marketing. Every capability below maps to what sponsors and CROs evaluate during site selection.

Phase I–IV & All Study Types
Full capabilities across Phase I through Phase IV, from first-in-human and dose-finding studies through post-approval surveillance. Equipped for interventional, observational, open-label, double-blind, and long-term extension studies across the network.
Phase I Phase II Phase III Phase IV OLE
Full Clinical Trial Support
End-to-end study management from startup through close-out. Investigator training, dedicated coordination and nursing support, regulatory document management, and complete site operations — coordinated across our Houston and Dallas locations.
Investigator Training Coordination Nursing Support Regulatory
Patient Recruitment & Retention
Multi-channel recruitment engine including physician referral networks, EMR-based pre-screening, community outreach, and digital advertising — deployed across Houston and Dallas to drive consistent enrollment at scale.
Physician Networks EMR Screening Digital Campaigns Community Outreach
Infusion Administration & In-House Pharmacy
Dedicated infusion rooms with IV infusion pumps and on-site infusion capability at each location. On-site investigational pharmacy with temperature-controlled drug storage and secure limited-access areas for IP management.
Dedicated Infusion Rooms IV Pumps On-Site Pharmacy Temp-Controlled Storage
Lab Processing & Diagnostics
On-site lab processing areas with refrigerated and ambient centrifuges, 12-lead EKG machines, vital signs and anthropometric measurement, and basic medical supplies. Access to local reference laboratories for sample analysis at each site.
Refrigerated Centrifuge Ambient Centrifuge EKG Local Lab Access
Safety & Emergency Readiness
Emergency cart, automated external defibrillator (AED), oxygen tank and cannulas, and trained medical staff on-site for every study visit. Houston sites benefit from proximity to the Texas Medical Center for immediate emergency care access.
Emergency Cart AED O₂ Tank & Cannulas Hospital Proximity
Rapid Site Activation
Average 6-week startup from site selection to first patient in. Central IRB, parallel contract/budget/regulatory processing, and experienced regulatory staff across the network eliminate common startup bottlenecks.
Central IRB Parallel Processing ~6 Weeks to FPI
Quality Assurance & Audit Readiness
Standardized QA processes across all network sites, regulatory document management, and audit-ready filing systems. Supports both remote and on-site monitoring. Staff experienced with FDA inspections and sponsor audit requirements.
Internal QA Remote Monitoring Audit Ready
Certified & Experienced Staff
All research staff GCP, IATA, and CCRP certified. Our team includes investigators, sub-investigators, research nurses, and coordinators with multi-therapeutic experience and low staff turnover across every site.
GCP IATA CCRP Low Turnover
Technology & Data Management
High-speed internet connectivity, EDC/eCRF workstations, CTMS integration, and secure limited-access areas for confidential documents at every site. Staff experienced across all major EDC platforms and sponsor portals.
High-Speed Internet EDC Proficient CTMS Secure Storage
Multi-Site Network Across Texas
Research sites in Houston and Dallas with centralized operations, shared SOPs, and unified quality standards. Place studies at a single site or leverage the full network for accelerated enrollment across two of Texas's largest metro areas.
Houston Dallas Centralized Ops Shared SOPs
Patient Experience & Retention Support
Patient meal services, bilingual staff (English/Spanish), comfortable waiting areas, and a supportive research environment designed to maximize visit compliance and long-term retention across your study.
Meal Services Bilingual Staff Patient Comfort Retention Focus

This is a summary of core network capabilities. Our sites are continuously expanding resources and services to meet evolving sponsor and CRO needs. Contact us for a complete site capabilities overview.

Network Diversity Profile

Built-In Diversity Across the Network

Diversity of study participants plays an important role. Inclusion of wide patient populations across races, ethnic groups, sex, genders, and ages provides evidence that study products or devices will be safe, effective, and generalizable across the broader target patient pool.

Network Race Profile
African American 40%
Asian 35%
Other 15%
White 10%
Network Ethnicity Profile
Hispanic 55%
Non-Hispanic 45%
90%

Minority Patient Enrollment

With sites across Houston and Dallas — two of the most racially and ethnically diverse metropolitan areas in the U.S. — our network demographics directly support FDA diversity enrollment guidance and Diversity Action Plan requirements.

Trusted by Leading Sponsors & CROs
AstraZeneca Novartis Sanofi Genentech Vertex Amgen Eli Lilly Biogen ACADIA Alexion Calliditas Prokidney Zenas BioPharma Dimerix Maze Therapeutics AstraZeneca Novartis Sanofi Genentech Vertex Amgen Eli Lilly Biogen ACADIA Alexion Calliditas Prokidney Zenas BioPharma Dimerix Maze Therapeutics
Partner With Us

Ready to Add a High-Performing Network?

Whether you're a sponsor placing a Phase I–IV study or a CRO looking for reliable, diverse, fast-activating sites across Texas — let's talk.

Request Network Capabilities Deck Call (346) 735-8990
contact@provectaresearch.org
Houston & Dallas, Texas