Purpose-Built to Speed Your Trial

For more than a decade, Alliance Clinical’s fully integrated, wholly owned and operated clinical research sites have helped advance human health by delivering exceptional clinical trial data gathered from a proprietary, ready-to-tap diverse participant population.

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We start with a database of 250,000+ consented patients from diverse populations

Our participant-focused sites bring innovative therapies to the people who need them most. Each location is affiliated with a local hospital, enhancing convenience for participants and researchers alike. Each fosters high participant engagement through a range of complimentary medical services. Each puts participants first. It’s one way we speed critical studies of innovative therapeutics.

Rapid Study Startup

Site selection to first participant screening in 35 days
Technology to quickly identify and contact appropriate participants
Proactive scheduling in anticipation of site activation

Audit-Ready Data

Standardized SOPS and technology
100% overnight QC on all visits
Track record of successful agency audits

Diverse Participant Population

>85% of database from underrepresented populations
Proactive focus on safety
Purpose-built sites in minority communities

Centralized management delivers consistent study execution across sites

Although our research sites span Texas, California, and Nevada, they share a single set of SOPs and a hands-on management approach. That strong oversight leads to steady, reliable results. It also means that best practices, from recruitment and retention strategies to reporting and audit preparation, are applied across sites to optimize support for your study.