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There are 3 ways that study related compensation / reimbursement can be provided to research study participants. The choice of options available for each applicable study are listed in the Informed Consent Document.

Please note that when using AU funds to compensate a research participant, the source of funds must originate from fund 15000 or any fund beginning with 2xxxx. Fund 10000 may not be used for any research participant compensation.

I.  PAYROLL

If an Â鶹¹ÙÍøÊ×Ò³Èë¿Ú employee participates in a research study, their study reimbursement is payable to them via payroll. These payments will be reflected on their W-2 to be in compliance with IRS regulations. The must be completed.

II. CHECK REQUEST

• 1. A check request may be used if the study provides only 1 payment to study participants.

• 2. Applicable IRB language must be included in the Informed Consent Document and is available in the .

• 3. The  and a   must be completed and forwarded to the Payroll Office. 

III. CLINCARD

• The ClinCard must be used if the study provides more than 1 payment to research participants provided that the participant is NOT an AU employee.

• A request for setting up the study in ClinCard must be submitted to clincard@augusta.edu by completing the  and attaching a copy of the IRB approved Informed Consent Document. Please note that the AU IRB approved language for the Informed Consent Document must be used and is found in the .

• The study visits and associated payment milestones will be set up in ClinCard by the Clinical Translational Finance Manager or other delegated Department Manager.

• Research participants must be consented prior to receiving a ClinCard or having payments issued. Upon completion of the approved consenting process, the study participant will be provided an AU ClinCard and a  sheet.  The participant will be required to complete a  and , which will be retained by the study site.  Visit payments can then be issued to study participant.  If travel reimbursement is due to the research participant, original receipts or appropriate travel documentation must be retained by the study site.

Often research studies provide payment or reimbursement to research participants. The amount of compensation may be minimal or in some cases research participants may earn thousands of dollars either through one high compensation study or through enrollment in multiple studies throughout the year. 

The IRS requires that individuals are responsible for reporting all payments to the IRS through their personal yearly tax return.  Â鶹¹ÙÍøÊ×Ò³Èë¿Ú is required to issue a Form 1099-MISC to any study participant who receives $600 or more per calendar year and report this payment to the IRS.  Box 3 on Form 1099-MISC is used to report “(a) payment or series of payments to individuals participating in a medical research study or studies.

Since AU cannot predict the total amount of total compensation that an individual may receive throughout the year (through participation in multiple studies), participants are required to provide personal information.  The amount and type of required personal information is detailed in the section below, Collection of Personal Information.  This information is used to ensure complete and appropriate reporting to the IRS in accordance with IRS policy.

There are some exclusions for IRS reporting: 

• If research study participant receives reimbursements, or payments (with receipts) to cover expenses incurred by the participant because of their clinical trial participation, (most often travel-related), then the payments are not considered taxable income.  These payments would not be included in 1099 reporting.
• If patient is diagnosed with a ‘RARE DISEASE’ and they are participating in a study providing treatments for this rare disease, they are allowed up to $2,000 per year without having the payment count as income that could jeopardize eligibility for Supplemental Security Income (SSI) and Medicaid.

Collection, via , of personal information (full name, address, and full social security number) is required for all research participants receiving compensation. This information is used to ensure appropriate oversight and compliance with IRS requirements. Waiver requests for consideration of alternative or limited collection of personal information may be requested.

Waiver Request Submission
Waiver requests for consideration of alternative or limited collection of personal information or alternative forms of research participant payment may be requested.  Requests for a waiver may be submitted for a study by using the .

Waiver requests must detail the following:

1. Reason for requesting the waiver
2. Who will be receiving the compensation? 
3. Who is the population for this study?
4. Alternative process for subject compensation that is being requested
5. Projected length of time for the completion of the study
6. Total amount needed to provide alternative compensation

 

Waivers will be reviewed by:

1. SVP Research or designee AND
2. AU Controller or designee

 

Decisions on authorizing a waiver must be unanimous.

There are normally two types of waivers that may be approved. The conditions for the waiver approval are listed below:

I.  Approved Waiver for Alternative Collection of Personal Information. Waivers approved under this category may include any of the following:

1. Waiver for entering the name, address, or social security number into the ClinCard system.
2. The collection of name, address, and full social security number of all participants receiving compensation must be collected and maintained in a log file as specified in the Waiver Authorization.
3. The collection of name and address and last four digits of social security number of all participants receiving compensation must be collected and maintained in a log file as specified in the Waiver Authorization.
4. The log files must be stored and saved by the PI, in accordance with AU Research Data Storage policies.
5. The log file must be provided to the Controller’s Office on a monthly basis to allow for oversight of IRS reporting requirements.
6. Inclusion of appropriate language in the IRB approved Informed Consent Document would be based upon the conditions of the waiver.

 

II. An Approved Waiver to authorize an alternative payment process. Waivers approved under this category would require that the following process is followed:

1. Â鶹¹ÙÍøÊ×Ò³Èë¿Ú currently subscribes to . This system allows gift cards to be sent electronically to study participants via email.
2.  In some situations, the electronic gift card may be printed by an AU employee and issued in-person to the study participant.  
3. The use of is only permitted via the issuance of a waiver and inclusion of appropriate language in the IRB approved Informed Consent Document.
4. For more information about this system or if your study may qualify for this type of study compensation, please contact clincard@augusta.edu.