At Valiance Clinical Research, we go beyond conducting trials—we cultivate trusted partnerships that shape the future of medicine. Every patient we support and every insight we uncover is driven by our unwavering commitment to advancing healthcare in meaningful ways. Grounded in scientific excellence and guided by compassion, we strive to create real-world change responsibly and ethically.
Collaborating with clients, Valiance conducts clinical studies across all phases of research and discovery, development, validation and approval. We add value across the full spectrum of clinical trials from fast and easy startups, dedicated recruitment staff for quick enrollment and retention, to capturing, reporting, and entering valuable data across applicable data capture systems.
To that end, our capacity and capabilities encompass the following:
Health research tests new treatments through clinical trials. Learn what’s involved.
We begin by sharing essential details about the study, what it’s trying to achieve, the treatment being tested, how long it lasts, and what your involvement might look like. You'll have time to ask questions and see if the trial is a good fit for you.
If you're interested in moving forward, we’ll provide a consent form that clearly explains everything, your rights, what’s expected of you, and any potential risks or benefits. There’s no pressure. You’re free to take your time, and even if you sign, you can withdraw at any point. Your comfort always comes first.
Next, we review your health history and may conduct a few tests to ensure the study is right for you. Every clinical trial has specific guidelines, and we take care to match participants carefully for their safety and the integrity of the research.
Once you're enrolled, you'll begin the trial. This may involve regular check-ins, health assessments, or treatment sessions, all designed with your safety and care in mind. Our team will support you closely throughout the process.
When the study ends, so does your active participation, but our connection doesn’t stop there. We’re here to answer follow-up questions, share what we can about the trial’s outcomes,and make sure you feel recognized and appreciated for the role you played in advancing science.
We begin by sharing essential details about the study, what it’s trying to achieve, the treatment being tested, how long it lasts, and what your involvement might look like. You'll have time to ask questions and see if the trial is a good fit for you.
If you're interested in moving forward, we’ll provide a consent form that clearly explains everything, your rights, what’s expected of you, and any potential risks or benefits. There’s no pressure. You’re free to take your time, and even if you sign, you can withdraw at any point. Your comfort always comes first.
Next, we review your health history and may conduct a few tests to ensure the study is right for you. Every clinical trial has specific guidelines, and we take care to match participants carefully for their safety and the integrity of the research.
Once you're enrolled, you'll begin the trial. This may involve regular check-ins, health assessments, or treatment sessions, all designed with your safety and care in mind. Our team will support you closely throughout the process.
When the study ends, so does your active participation, but our connection doesn’t stop there. We’re here to answer follow-up questions, share what we can about the trial’s outcomes,and make sure you feel recognized and appreciated for the role you played in advancing science.
It is important that culturally and linguistically diverse people have access to clinical research to ensure that the evidence gathered is applicable to them. We know that there are potential factors such as racial differences in opioid receptors, cultural expression of pain, interaction with healthcare professionals, perception of interventions or hospital admission that may impact this. This is why it’s critical to have diverse representation in clinical trials – to better understand patient differences that may affect clinical outcomes. Our patient demographics consist of the following:
Hispanic or Latino: 46.9% of the population
White (non-Hispanic): 28.9% of the populationn
Asian: 11.7% of the Local population
African American: 8.3% of the population
Two or more races: 3.3% of the population
Other: 0.7% of the local population
Failure to meet enrollment targets or population diversity can compromise data quality and regulatory acceptance. Our sites achieve a 97% retention rate through frequent check-ins, text reminders, and personalized engagement. We meet 98% of enrollment goals, with 80% from internal databases, 10% from referrals, 5% from community events, and 5% from digital marketing.
We utilize our deep medical expertise and insights into gaps in patient care to help develop cutting-edge therapies and innovative solutions. By focusing on essential therapeutic areas, we aim to address complex diseases and expand treatment options, ultimately enhancing patient outcomes and improving quality of life. These therapeutic areas are the following:
Our expert teams work closely with sponsors to tailor the best solution for each project.
We have expertise in conducting clinical trials and the efficacy of treatment for a wide range of conditions.
Valiance Clinical Research combines expertise, agility, and proactive strategies to optimize clinical development and help deliver impactful therapies to patients
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