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REFER FAMILY AND FRIENDS - STUDY 0035-0731
Refer your family and friends and earn up to $500*
If you have a friend or family member who wants to participate in one of our studies, you can add them here. When he or she qualifies, you may be eligible for a referral bonus of up to $500*.
You must have previously registered with ICON to refer family members and friends.
STEP one
Tell us a little about yourself so that we can create a unique ID, which allows us to link you to your referrals.
STEP two
Add your friends' email addresses to refer them for one of our studies.
*Have you previously registered with ICON?
*Please select the clinic that's right for your family members and friends.
*Please enter your family and friends' email addresses:
We’re missing something. Please review the information you’ve provided.
We are committed to keeping your personal information safe and secure. Please see our Privacy Notice.
ICON Referral Program Guidelines:

Receive compensation simply by telling others about our clinical research opportunities at ICON.

  • The referred participant must dose in a study. Since the participant may not qualify for the original study for which they were referred, the referral stipend will still be paid if the participant doses on a study within 12 months*.
  • There is no limit to the number of first time participants you can refer for a study and you do not have to be a study participant to refer others for our studies.
  • Your referred participant must mention your first and last name during the pre-screening over the phone in order for the referral stipend to be paid.
  • The referred participant must fill out a referral card at the screening visit so that we can document the referral. This step is a key requirement for paying out the referral stipend.
  • If you refer a new first-time participant who doses, you could receive up to $500; there is no limit to the number of participants you can refer to our studies, however they must be first-time participants.
  • You will be paid via ClinCard within four weeks from the date the referred participant received study medication.
  • ICON reserves the right to change, amend, modify, or terminate this referral program at any time and is subject to IRB approval.
Notes:

**Screening nor receiving the drug during the discrimination phase (if applicable) does not constitute as being dosed in the study. Qualifying and receiving the study treatment constitutes dosed. If you need further information on this requirement, please contact the site you referred the participant to. For more information, click here to send us an email or to give us a call.

Actual study participant
Lenexa, KS
“Enjoyed my stay and the staff are wonderful.”
Actual study participant
Lenexa, KS
“All employees were extremely courteous and helpful.”
Actual study participant
Lenexa, KS
“Wonderful staff. I am a newbie, but friendly and helpful staff eased the apprehensions.”
Actual study participant
Lenexa, KS
“ICON has an excellent staff from recruiters to medical staff, and a nice, clean facility.”
Actual study participant
Lenexa, KS
“It looks to me like ICON staff is courteous and very knowledgeable of the proceedings and well-being of every participant.”
Actual study participant
Lenexa, KS
“The staff at ICON is wonderful. Very professional and friendly.”
Actual study participant
Lenexa, KS
“Staff is friendly and professional.”
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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.
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