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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.
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.
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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What is a clinical trial?Clinical trials are research studies that explore whether a medicine, treatment, or device is safe and effective for humans. These studies also may show which medicine, treatment or device works best for certain illnesses or groups of people.
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Who can participate in a clinical trial?We recruit healthy volunteers and patients. Healthy volunteers are typically between 18 and 65, take no medications and are generally healthy. Patient clinical trials generally include people with a specific medical condition. The eligibility requirements usually vary between each trial. Any participation is voluntary and each trial has requirements as to who can enter the trial.
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Will there be any cost to me if I participate in a clinical trial?Trial-required medications, study visits, and any medical tests specifically needed are provided at no cost to you or your insurance company. Time and travel reimbursement may also be possible for qualified participants. Information about other potential benefits is included on this website and in the informed consent form and the study team will answer any questions about cost that you may have.
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How many visits should I expect?This will vary depending on the clinical trial. The Informed consent form (ICF) will detail the visit schedule and what will occur at each visit. The study team can also answer any questions.
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Can a participant leave a clinical trial after it has begun?Yes. A participant can leave a clinical trial at any time. When withdrawing from the trial, the participant should let the research team know. Clinical trials are completely voluntary and participants can leave the trial at any time for any reason. There is no penalty or fee of any kind for withdrawing.
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What happens after my trial is completed?When you finish a clinical trial, you may have many questions. Your clinical research coordinator is in the best position to help you plan what to do next. Regardless of next steps, make sure to request a copy of your medical information collected during your participation in the trial. That will be important for doctors you may see in the future.
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.
How clinical trials work - Health research tests new treatments through clinical trials. Learn what's involved.
1. Pre-Screening
First, you will learn about the trial. This may be done via online education, through a contact center, or at an appointment with the local research team. This education usually includes an understanding of you (and if appropriate, your match to 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.
2. Informed Consent
You will be provided with a document that details what you need to know as a trial participant so you can make an educated (informed) decision on whether you would like to take part in the trial. The clinical research coordinator will review the document with you and answer any questions you may have. You may want to bring a family member or friend to your appointment to help write down answers to your questions. If you decide to participate in the trial, you will sign the form, which provides your consent and acknowledges your understanding of the risks and your responsibilities. Even if you sign the consent form, you may withdraw from the trial at any time.
3. Screening
The informed consent form covers topics such as:
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Purpose of the research
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Who is eligible to participate
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Expected length of time for participation
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A description of the procedures (exams, tests, etc.) that will be part of the trial
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A description of any expected risks
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Possible discomforts (e.g., injections, frequency of blood tests, etc.)
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Handling of data (e.g., confidentiality, record keeping, FDA inspections)
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Who covers the cost if a clinical trial causes an injury
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Participant rights (e.g., the right to stop participation at any time)
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Who to contact if you have questions
During a participant screening visit, the research team will review your medical history and conduct any other procedures and tests (such as blood work, vitals, body measurements, biopsies, or scans) to make sure you meet all requirements to join the trial.
4. Enrollment and Participation
If you qualify, your participation can begin. The research team will provide detailed instructions on what you may need to do at home, how often you will need to visit the trial site, and what will be required at the visits (e.g., physical exams, questionnaires, tests, and procedures). Your overall health and safety are continually monitored for the duration of the trial. Taking part in a trial may require more doctor visits than usual, however many trials offer some reimbursement for your participation.
5. End of Trial Participation
Each trial has predefined trial completion criteria. When you complete your trial participation, you may meet with your regular healthcare provider, if different than your research team, to determine further care options. If you are a healthy volunteer, your commitment is over. Keep in mind that researchers can decide to end trials earlier than expected for a variety of reasons. You may also withdraw your consent to participate at any point during the trial.
Enhancing Healthcare For All
How to Participate in a Clinical Trial
To participate in our clinical trials, please register your details with us. This allows us to match you with a trial that fits your profile. Each study has specific eligibility criteria, including height, weight, and BMI requirements. Once registered in our database, we will review your information and notify you of suitable trials, including their purpose, eligibility requirements, and schedule.
The Benefits of Participation
Have you ever considered participating for a clinical trial, but felt unsure? There are numerous benefits to volunteering. We have highlighted a few reasons why you should participate in a clinical trial. These include the following.
Your participation matters and is a key part of medical innovation and advancement.
Learn more about your illness or condition. You may have the opportunity to receive diagnostic tests & exams at no cost.
Many clinical trial pay for your time and effort spent during the study. Compensation varies and is often contingent upon study length and requirements.
Many people hesitate to participate due to lack of insurance. Insurance is not required to participate. In addition, participating in a clinical trial may give you access to medication and care that previously felt unavailable.
Participating in clinical trial may give you access to cutting edge treatments and medical innovation at no cost and therefore your overall health may improve. In addition to studying the effectiveness of a treatment, researchers may also be investigating other aspects of care to improve the quality of life for people with chronic illness.
Phase II-IV clinical studies often require visits with a doctor who is an expert in the disease area being studied. Moreover, this study related care can help you learn valuable insights into your health with no long wait list or waiting rooms!
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.
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Valiance Clinical Research combines expertise, agility, and proactive strategies to optimize clinical development and help deliver impactful therapies to patients
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