Participants Registration

Expect your experience at Phoenix Research Center to be professional, warm, and always confidential.

“United to help improve people health for a better tomorrow.”

The purpose of clinical research is to determine how new medications and treatments work on people. By conducting clinical trials or studies, doctors help discover new and diverse ways to detect, diagnose, control, treat, and even prevent illnesses. Before a new medication or treatment is approved for use by the public, it is necessary to test it in detail according to the strict rules and regulations of the U.S. Food and Drug Administration (FDA).

Clinical Research studies are being conducted at Phoenix Research Center. On this site, you’ll find more information about clinical research studies available and that may be of interest to you or a friend. Look around and find out if you could be a part of the future of medicine.

We are currently recruiting volunteers to participate in our research studies. To learn more about these investigational medications that are not yet available to the public please use the registration form below to see if you qualify. With your help, doctors and researchers can gain a better understanding of these investigational medications bringing new hope for patients afflicted with different conditions and diseases.

Information For Prospective Participants

  • No health insurance required.
  • Volunteers are compensated.
  • Receive health benefits such as study-related medical care, diagnostic testing, medications, and more at no cost.
  • The purpose of clinical trials is to evaluate the effectiveness and safety of new medications. By volunteering now, you are helping alleviate the pain of future generations.
  • Our location provides easy access and ample parking, which is convenient for study participants and visitors.

Client Study FAQ

Once you are eligible and agree to participate in a study, you will be asked to visit our clinic a certain number of times, depending on the length of the study. You may also be asked to stay overnight. If you are asked to stay overnight, you will be provided with a room and meals. During your study clinic visits, study doctors and staff members will evaluate your health and response to any medication you have been given. Some of the tests and assessments they may use include: *Reviews of your medical history *Physical exams *Vital signs measurements *Blood and urine sample collections
Once you are eligible and agree to participate in a study, you will be asked to visit our clinic a certain number of times, depending on the length of the study. During your study clinic visits, study doctors and staff members will evaluate your health and response to any medication you have been given. Some of the tests and assessments they may use include: Reviews of your medical history Physical exams Vital signs measurements Blood and urine sample collections Questions about how you are feeling Reviews of any medications you are taking Reviews of any side effects you experience Study doctors and staff members will go over all tests and assessments. You will be encouraged to ask questions about anything you don't understand.
A clinical trial is a research study conducted in human beings with the goal of answering specific questions about new therapies, vaccines or diagnostic procedures, or new ways of using known treatments. Clinical trials are used to determine whether new drugs, diagnostics or treatments are both safe and effective. To obtain FDA approval, the company that makes the medication or device is required to conduct clinical research studies. The companies ask people to volunteer for clinical research studies. In these studies, volunteers are given the investigational medication or device and are evaluated by study doctors and staff members. After clinical research studies are completed, the pharmaceutical company then submits the study information to the FDA. The FDA reviews this information and decides if the investigational medication or device can become available to the public. The FDA does this to learn more about the product and make sure that it is effective and safe.
You will be paid for your time and participation in the study. Compensation is based on the length of the study, the number of overnight stays in our clinic, and the number of outpatient visits you attend. How will I receive payment for my participation? Payment details will be discussed with your clinical study team at your first visit. We offer payment by check and direct deposit. How many paid research studies can I do? After you've finished a clinical trial, you usually must take a 1-3 month break. The length of time depends on requirements for the study you would like to enroll in next. If you have questions about your eligibility for a trial, please call us at
You have clearly defined rights at all stages of a clinical trial. Before a trial, you will be given information to help you make the best decision for you about whether you participate in the trial. You will also have informed consent. You will understand the benefits, risks, study length, where it will be conducted, and what will be expected of you during the trial. You can and should ask questions and talk about any concerns you have. You can decline participation or withdraw from a study at any time. You will also be apprised of any findings that come out during the study that may affect your participation. Your medical information and data will be kept strictly confidential. HIPAA Privacy rules apply to clinical research. You also have the same Patient Bill of Rights that any other patient receiving medical care can expect. Your team of researchers and medical care providers have a legal, ethical, and safety responsibility.