FAQs

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.

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.

Participant safety is the top priority. Clinical trials are reviewed and approved by an independent ethics committee (IRB) and often monitored by the FDA or other regulatory agencies. You will be closely monitored by medical professionals throughout the study, and your health will always come first.

Some studies include a placebo (a substance with no active medication) for comparison purposes. If a study includes a placebo, this will be clearly explained to you during the consent process. You will have the opportunity to ask questions before deciding whether to participate.

No. Study-related medications, tests, and medical visits are provided at no cost to you. Participation in a clinical trial should not require you to pay for study-related care.

Many studies provide compensation for time and travel. Compensation varies by study and will be explained before you decide to participate.

Health insurance is not required for most clinical trials. Study-related care is typically provided at no cost to you.

Yes. Participating in a clinical trial does not replace your primary care physician. In many cases, your regular doctor can continue managing your general health while the study team oversees study-related care.

Participation is completely voluntary. You may choose to leave the study at any time, for any reason. Your decision will not affect your regular medical care or benefits.

Each study is different. Some studies last a few weeks, while others may continue for several months or longer. The expected time commitment will be clearly explained before you enroll.

Each study has specific eligibility criteria based on age, medical history, and other factors. The best way to find out if you qualify is to complete the eligibility form or speak with a research team member.

Your privacy is very important. Clinical trials follow strict confidentiality and HIPAA guidelines to protect your personal health information. Your data is handled securely and shared only as required for research purposes.

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).

Once you submit the form, you’ll be contacted by a volunteer recruiter from the PRA 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.

At the first screening visit you will receive 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.

You can find clinical studies by clicking here: Find a Study