Let’s unite to transform the patient experience and redefine the landscape of clinical trials.

Optimized Start-Up Process

At RIO Clinical Trials, we accelerate study start-up with a streamlined, tech-enabled approach. Our digital systems for source, regulatory, and record management help launch and scale even complex trials fast.

We support specialized, decentralized, and hybrid studies, integrating smart tools for payments, data, and coordination. From award to site activation in under 30 days, our team ensures smooth IRB/lab alignment and site staff training.

Meet Enrollment Goals

RIO Clinical Trials delivers on enrollment and retention especially in high-volume or challenging studies. Our tech team continuously improves recruitment, screening, consenting, and retention for Sponsors, CROs, and participants.

Each site has dedicated recruitment staff and is located in diverse communities to ensure broad representation. We provide exclusive access to physician/practice databases, rapid enrollment support, and strong outreach and diversity programs. Our in-house advertising surpasses central campaigns, and our adherence programs and specialty care sites help reach unique populations and support complex procedures.

Rigorous Oversight & Data Management

RIO Clinical Trials leads with a high-standard quality oversight model. Our in-house team’s clinical data, QA, regulatory, and risk management work hand-in-hand with site staff to ensure full compliance with FDA, ICH GCP, state laws, industry standards, and our own strict SOPs.

We target 48-hour data entry and query resolution, with regular QA reviews, EDC/source checks, and continuous training for investigators and staff. Our sites are supported by CLIA-certified labs, IATA-certified personnel, and GCP-trained professionals.

For Sponsors

RIO Clinical Trials offers a network of experienced investigators across diverse specialties and locations. Our model ensures high-quality, reliable, and efficient execution even for complex trials.

Partner with us to elevate the quality and impact of your clinical research.