Driving Innovation in Healthcare

We manage all stages of clinical research – from initiation to close-out – with a therapeutic focus and a patient-centered approach, advancing better health outcomes for all.

Your Research, Accelerated

An evidence-based approach

Providing a blend of expertise, scalability, agility, and proactive engagement across all phases of clinical development.

Our Mission

Our mission is to advance medical knowledge and treatment with a patient-centered approach by offering innovative, personalized therapeutic options that enhance lives and positively impact patient outcomes, driving meaningful change in healthcare.

Our Values

We are committed to core values of innovation, inclusivity, integrity, compassion, respect, trust, collaboration, safety, quality, and patient empowerment, ensuring excellence in healthcare and fostering a supportive environment for all stakeholders.

Our Team

Our leadership team consists of diverse, experienced professionals from various disciplines, united by a shared passion for delivering exceptional patient care and driving excellence in healthcare services through collaboration and innovation.

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The Clinical Trial Participant Journey

Participating in a clinical trial is a voluntary decision, and you can choose to withdraw from the trial at any time if you change your mind. Before you enroll, you will go through a series of steps to ensure you meet the requirements of the trial and are informed about the risks and responsibilities of participating. This process will help you make an educated decision.

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Help Advance Medical Science

Human clinical trials are an essential component of medical research, playing a pivotal role in evaluating the safety and efficacy of new treatments. Our extensive network of healthy participants contributes to these studies for a variety of personal and scientific reasons. Regardless of your motivation for considering participation, it is important to ensure that a clinical trial aligns with your individual needs and circumstances. Participation is entirely voluntary, and you retain the right to decline enrollment or withdraw from a study at any time, should you choose to do so.

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Research-driven, People-Focused Healthcare

Valiance Clinical Research is a leader in advancing research aimed at preventing and treating diseases that impact people’s health through clinical trials. We strive to provide educational, informative, and transparent content for all. To those who have joined a clinical trial with us or are considering enrollment, we extend our heartfelt thanks and appreciation. Your partnership is essential as we work to develop groundbreaking new medicines and therapies.

How clinical trials work

Health research tests new treatments through clinical trials. Learn what’s involved.

Pre-Screening

First, you will learn about the trial.the trial’s purpose, treatment information, potential benefits and risks, the length of your participation, and an overview of the trial’s activities.​ Read more

Informed Consent

You will be provided with a document that details what Even if you sign the consent form, the you may it withdraw from the trial at any time.​ Read more

Screening

  • Purpose of the research
  • Who is eligible to participate
  • Expected length of time for participation
  • Read more

  • Enrollment and Participation

    The duration of the trial. Taking part in a trial may require more doctor visits than u.​ Read more

    End of Trial Participation

    your commitment is over. Keep in mind that than expected for a variety of it is of a with reasons. Read more

    The importance of diverse participants

    Individuals can respond differently to the same medication depending on factors such as age, gender, weight, race, ethnicity, and more. Clinical trials depend on the participation of volunteers to determine if medicines and vaccines are safe and effective across diverse communities.

    The Benefits of Participation

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    Our Commitment 

    The importance of diverse participants

    Individuals can respond differently to the same medication depending on factors such as age, gender, weight, race, ethnicity, and more. Clinical trials depend on the participation of volunteers to determine if medicines and vaccines are safe and effective across diverse communities.  

    Frequently asked questions

    What is a clinical trial?

    Clinical trials are research studies that explore whether a medicine, treatment, or device is safe and effective for humans.

    Anyone may be eligible to participate in a clinical trial depending on the specific requirements of the study. Each trial has inclusion and exclusion criteria based on factors like age, gender, medical history, current health status, and sometimes lifestyle habits. At Valiance Clinical Research, our team conducts a thorough screening process to ensure participants meet the necessary guidelines. If you’re interested in contributing to medical research and improving future treatment options, contact us to see if you qualify for one of our ongoing clinical trials in Los Angeles.

    No, there is no cost to participate in a clinical trial at Valiance Clinical Research. In most cases, participants receive study-related medical care, lab tests, and investigational medications at no charge. Additionally, many trials offer compensation for time, travel, and participation. Our team will provide all financial details during the initial screening so you can make an informed decision.

    The number of visits required depends on the specific clinical trial protocol. Some studies may require just a few visits over several weeks, while others may span several months with more frequent check-ins. At Valiance Clinical Research, we prioritize transparency and will clearly explain your visit schedule before you enroll. Our goal is to make participation as convenient and manageable as possible.

    Yes. Participation in any clinical trial is completely voluntary, and you may withdraw at any time and for any reason. Your decision to leave will not affect your access to medical care or your relationship with our staff. At Valiance Clinical Research, we support our participants’ autonomy and are committed to your comfort and safety throughout the process.

    After your clinical trial ends, you may be asked to attend a follow-up visit for final assessments. The data collected during your participation will be analyzed to help advance medical research and improve treatments. In some cases, you may be updated on the outcomes of the study, though full results are often published after all phases are completed. At Valiance Clinical Research, we value your contribution and will guide you through any post-trial procedures.

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