Our Clinical Trial Site

Every breakthrough begins with volunteers like you — together, we’re transforming healthcare for generations to come. If you’re interested in joining a study, call our office at (657)-216-1255.

What To Expect When You Join a Trial

Participating in a clinical trial is simple and supportive — here’s what you can expect, step by step. From your first visit to follow-up care, we’ll guide you through every stage.

Screening & Enrollment

You’ll first meet with the research team, who will explain the study in detail, answer your questions, and check if you meet the eligibility criteria. This may include a review of your health history, a physical exam, or lab tests. If they determine that you are eligible, you will sign consent forms and will be enrolled into the study.

Study Visits &
Care

If you qualify, you’ll attend scheduled visits at the clinic. During each visit, you’ll receive the study treatment (or placebo, depending on the design) and undergo check-ups, tests, or questionnaires to track your health and progress. The team will closely monitor your safety and well-being at every step.

Follow-Up &
Results

You’ll first meet with the research team, who will explain the study in detail, answer your questions, and check if you meet the eligibility criteria. This may include a review of your health history, a physical exam, or lab tests. If they determine that you are eligible, you will sign consent forms and will be enrolled into the study.

Our Trial Management Solutions

At Triallogix, we've helped research sites like yours successfully navigate regulatory compliance for over 500 studies --and counting.

Our Solutions

IRB Submissions & Oversight

By streamlining submissions, minimizing delays, and safeguarding against compliance risks, we can help you activate studies faster, maintain audit readiness, and build trust with sponsors and participants. Our expertise keeps your trials running smoothly, protects your site’s reputation, and positions you as a preferred partner for sponsors, all while saving you time and resources to focus on quality research.

Our Solutions

Regulatory Document Management

Stay audit-ready at any moment --with us, your site’s regulatory documents will be meticulously organized, compliant, and ready for audits at any time. By ensuring every essential document is accurate, up-to-date, and easily accessible, we help you avoid compliance risks, maintain strong relationships with sponsors, and meet regulatory standards with confidence.

Frequently
Asked Questions

Have questions about joining a clinical trial? Here are some of the most common things people want to know before they participate.

1. What is a clinical trial?
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2. Is it safe to participate?
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3. Will I get paid or receive medical care?
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4. How much time will it take?
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5. Can I still see my regular doctor?
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