Frequently asked questions
Frequently asked questions
About clinical studies
What happens in a clinical study?
During a clinical study, you’ll receive the medication that is being studied. This will be done at scheduled times and may occur only once or multiple times throughout the study, depending on the medication. If you participate, you may also have the following procedures performed to monitor your health: vital signs, blood work, physical exams or other types of assessments that are necessary to gather the required information about the study medication. In some studies, you may not receive the study medication, but instead receive a placebo (a substance having no pharmacological effect but administered as a control). All study volunteers are closely monitored by our clinic staff and medical team to ensure their safety at all times.
Who can participate in a clinical study?
Each clinical study has requirements for participants based on specific factors such as age, medical history and current health. The eligibility criteria in each study protocol are used to identify the volunteers best qualified to participate.
Where are clinical studies conducted?
ICON conducts clinical studies at three sites in the United States – Lenexa, KS; Salt Lake City, UT; and San Antonio, TX. For in-house studies, volunteers stay in the clinic during the study and may not be allowed to leave the premises due to safety monitoring. Out-patient studies do not require overnight stays.
Are clinical studies safe?
Most clinical trials may involve some risk. Side effects are possible when taking medication, however, the safety and well-being of participants is always our No. 1 priority at ICON. ICON has been successfully conducting clinical trials for more than 32 years and has an excellent safety record. Read more about Safety & Privacy here.
Why should I participate in a clinical study?
Participating in a clinical study is a great way to help with the development of new and improved medications. As a study participant, you may be eligible to earn reimbursement for your participation and time.
How do I find out about clinical studies?
You can learn more about our clinical studies by clicking here or by calling one of our recruiting offices at: Lenexa, KS: 1-913-259-7100 1-913-259-7100 Salt Lake City, UT: 1-801-269-8200 1-801-269-8200 San Antonio, TX: 1-210-225-5437 210-225-5437
What questions should I ask before agreeing to participate in a clinical study?
You have the right to ask any questions before, during or after volunteering. Some questions may include: What is the intended use of the drug? What are the risks? What are the benefits? What will I need to do? How long does the study last?
What is an Informed Consent?
An Informed Consent is a process that explains the details of the study, including the potential risks and benefits, as well as your rights and responsibilities. You will be provided the facts about the study to help you determine if you want to participate in the study. This includes details and possible side effects of taking the investigational product (medication).
How am I protected if I decide to participate?
Every clinical trial in the United States must be approved and monitored by an Institutional Review Board (IRB) to make sure the risks are as low as possible and are worth any potential benefits to the volunteer. As a volunteer, you have the right to discontinue your participation and leave the study at any time and for any reason, with no penalty or loss of benefits to which you are otherwise entitled to.
Will I be paid for taking part in a clinical study?
While participation in a clinical study is voluntary, you may be reimbursed for your time and travel. Compensation is based on the length of the study, the number of overnight stays, the number of out-patient visits you attend, and also based on risk. You may also be compensated for specific procedures depending upon the study. All payments we make for study participation have been approved by an Independent Review Board (IRB). The method and frequency of payment will be described in detail in the Informed Consent Form (ICF).
What happens once I fill out the application form?
Once you submit the form, you’ll be contacted by a volunteer recruiter from the ICON Recruiting Department. The recruiter will discuss available studies and ask you a few more questions to make sure you meet the eligibility requirements of the study. If you do, the next step will be to schedule a screening appointment.
What happens at a screening appointment?
You are provided with detailed information about the study and can decide at any time if you wish to continue to participate. Several tests may be performed such as vital signs, physical exam, blood work, questionnaires, or others to determine whether you qualify for the study. If your information and results match the requirements for the study, you may be given the option to participate.
What can I expect if I participate in a study?
Here’s a brief overview of what you can expect. Safety & Privacy here.
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About ICON
We’re committed to the drug development process because we understand how it impacts the lives of patients and their families. At the end of the day, we’re not just researchers. We’re patients. We’re survivors. We’re family members.