Clinical Research Solutions for Real-World Sites
Helping investigators, coordinators, and healthcare organizations build reliable, compliant, and efficient clinical research operations.
Our Services
We provide professional clinical trial operational services to enhance your clinical research site. Building on over 15 years of experience, we will work with your team to develop workflows to ensure you stay compliant and a top-performing site for your sponsors and patients.
Regulatory & Compliance
We review regulatory (e)binder, identify gaps, and build structures that keep your studies inspection-ready. From IRB submissions to consent documentation to essential binder organization, we help ensure your compliance holds up under scrutiny.
Study Startup & Operational Support
We help sites launch studies with clarity and purpose. That includes pre-study activities, workflow mapping, budget review, delegation log setup, and the practical steps that keep startup on schedule and reduce downstream confusion.
Data Review & Workflow Optimization
We evaluate how data flows through your site, surface accuracy or consistency issues, and develop cleaner processes for entry, review, and maintenance. The goal is to reduce errors, eliminate rework, and create data you can trust on initial entry.
Training & Team Development
We design training that actually sticks. It’s interactive, clear, and built around the realities of busy research teams. Whether you need onboarding refreshers, protocol-specific training, or help bridge knowledge gaps, we can make learning simple and sustainable.
Quality, Auditing & Site Readiness
We support internal audits, mock inspections, CAPA development, and quality reviews that identify risks before they become findings. Rather than rely on a NTF, we take those important and necessary steps to help teams build confidence and stay consistently inspection-ready.
About Us
Cordova Clinical Research was founded in 2025 in Southern California with a simple mission: strengthen research sites by building cleaner, processes, tighter compliance systems, and internal standards that hold up under real-world pressures. We believe every site cab operate with more clarity and less chaos, and we focus on developing procedures that keep teams consistent, confident, and always ready for an audit.
Our approach starts with listening. We study the workflows already in use, pinpoint what’s effective, and uncover the gaps that quietly slow everything down. Then we fill those gaps with clear tools, hands-on training, and the kind of practice activities that make concepts stick. The aim is to strengthen the whole operation with smoother processes, sharper adherence to compliance, and teams that feel truly supported.
Why Us
We realize that most sites don’t need more clinical research theory. They need practical solutions that bring real results. We focus on the real problems like antiquated workflows, shaky compliance, confusing role delegations, and endless sponsor or monitor requests. Our job is to bring order to your sites and strength the systems you already have.
Who we serve
• Investigators and clinicians who want reliable research support without sacrificing patient care or compliance.
• Research coordinators and managers who need operational clarity, training, and systems that help—not hinder—their workload.
• Hospitals and research organizations looking to expand or strengthen their research programs.
• New or growing research sites that need guidance on building their processes from the ground up.