
FAQs
Frequently asked questions about participating in a Medpace clinical trial at the Phase I Unit
Frequently asked questions about participating in a Medpace clinical trial at the Phase I Unit

Frequently asked questions about participating in a Medpace clinical study
Read our FAQs that provide study participant information for Medpace clinical studies.
Don’t see your question listed? Contact our call center to learn more about participating in a paid clinical trial at Medpace.
When you participate in a clinical research study, you can change the pace of medicine. Research participants are critical in the development and testing to find better ways to diagnose and treat patients. Your participation in a study helps move this process forward to finding new therapies for critically ill patients. As a participant in a study, you may be eligible to receive compensation for your time and travel.
Volunteering for clinical studies may not only benefit you, but could benefit millions through the development of life-changing treatments.
At Medpace, our goal is to advance medical knowledge and help bring new treatments to the public. Before a drug or device can be introduced to the public, it must undergo a series of studies to prove that it is safe and effective. We have conducted hundreds of Phase I Studies and have built a staff of qualified and experienced professionals who work to safely manage our studies.
Participants must complete the Study Participant Questionnaire to take part in a Medpace clinical study. The Medpace Clinical Pharmacology staff will determine your eligibility for current or future studies based on your medical history and the answers you provide in our questionnaire. Your answers are kept completely private and are not shared with anyone else.
After you become a registered participant, a Medpace staff member will work with you to schedule a screening appointment. Following your screening appointment, you will go through the informed consent process, receive a complete medical examination, and then, depending upon the study, you may undergo blood/urine testing and other routine procedures to confirm you are in good health prior to enrollment.
Every study is different. There are a multitude of reasons as to why you may not be chosen for a study. If you do not qualify for a specific study right away, we will keep your name in our confidential database, and contact you when we have a study that is a good match for you.
Informed Consent is an agreement between you (the study participant) and the study’s Principal Investigator (PI), designed to ensure your safety and guarantee that you fully understand the risks involved before you volunteer to participate in the research study.
Yes. As you will learn during the Informed Consent process, participants are allowed to withdraw their consent for study participation at any time. You may also ask to have your name removed from our database and we will stop contacting you for any future potential study participation.
All study participants must be honest with the study staff, and follow all guidelines throughout their stay. This is for your own safety.
The Medpace Phase I Unit does not have a visiting area, so during your stay your contact with friends and family is limited to text, phone, email, or internet applications like Skype®.
Staying overnight at Medpace provides the most controlled environment for a Phase I or Phase IIa study. This includes the ability to standardize meals, activities, medication dosing, taking blood/urine samples, special testing, and monitoring for adverse events. The duration of your stay is designed for your safety.
In order to make your stay as comfortable as possible, the Medpace Phase I Unit features:
- Recreation rooms outfitted with widescreen televisions, board games, and other activities
- Personal TVs, cable channels, access to Netflix®
- Desktop computers
- Wireless technology for personal phones, pads and laptops
- Video games (Xbox 360®)
- A well-lit, secure outdoor courtyard (weather permitting)
- Catered meals
Each available clinical study lists the amount you could be paid for your participation and travel.
