Technical Support:
Data Subject Rights and Compliance:
Getting Started With StudyTeam:
StudyTeam Functionalities:
To rest your password:
Please follow the steps below if you receive Data Subject Access Requests (DSAR) on behalf of your patients for any of the following:
You can find more information about your data subject rights under Section 6 of our Privacy Policy.
Please note: if you as a site have the operational need to remove patients from the Trial Board and Patient Log view, this is not a DSAR-type request. This is simply an operational removal of patient data from view and can be accomplished by moving the patient tile to "Archive" status on the Trial Board.
If you have a specific Data Subject Access Request (DSAR) for how you want us to handle your personal data, please reach out to privacyofficer@onestudyteam.com with this request. Our privacy team will connect with you to ensure your data privacy rights are met. You can also find more information about how we handle your personal data in our Privacy Policy.
If OneStudyTeam's Customer Success Team representative contacted you with an opportunity to work in StudyTeam on a trial whose Patient Log is directly connected to the respective sponsor team in a de-identified way, you can take advantage of this option in two ways.
Upon instruction from your Customer Success Team representative, you can give your consent for them to sponsor-connect the trial on your behalf. They will ensure that the your prescreening log for the respective study is shared with your sponsor in real-time and in an automatically de-identified way.
Alternatively, if you prefer to request the sponsor connection yourself inside the app, please follow these steps here.
Who owns the data?
You -- the site -- own all the data you enter into StudyTeam.
What do you do with the data?
The data you enter is shown to you when you log in. Whatever is entered goes into how StudyTeam serves you and the more that you use StudyTeam, the more useful it gets to be for you.
Do you sell my data?
Absolutely not. All data is confidential and we maintained the utmost standards for security.
Instead of a paper checklist for pre-screening patients, OneStudyTeam can configure an I/E criteria checklist for any of your trials within StudyTeam that you will be able to use to pre-screen patients. This will help you stay organized and screen potential patients more efficiently!
Send an email to support@onestudyteam.com to set this feature up for your trial.
In any instance that you (or your site) might need to generate a System Access report for StudyTeam for Sites, please follow these steps:
The system access report will contain information about every StudyTeam for Sites user that has had access to Trials at your site, when access was granted, and when it was revoked (if applicable).
Each site is the Data Controller of their StudyTeam for Sites system and therefore the only ones that are able to request a system access report.
Let your sponsor know that you are using the newest technology to help track and organize your recruitment and enrollment process. StudyTeam helps sites enroll every enrollable patient. By introducing your sponsor to StudyTeam, you are letting them know that you are ahead of the game in terms of recruiting and prescreening.
Learn some ways that working with more sponsors in StudyTeam can save you time and improve your recruiting process in this article.
See a full list of countries and languages here.
Our support team is standing by to help you. If you have a question, please contact us by submitting a support ticket.
If you would like to freshen up your StudyTeam skills, schedule a time to speak to us by clicking here:
Back to the topBefore contacting StudyTeam support, check if your issue can be resolved by one of the common conditions listed here.
Back to the topBoth the full Inclusion/Exclusion criteria list and the Inclusion/Exclusion checklist that you can customize yourself can be easily printed from your StudyTeam platform.
Both the full list list and the checklist you customize are available under the Patient Profile.
When you navigate to and click on the "Prescreening Checklist" icon on the Patient Profile, this will take you to a table which allows you to either consult the full list of Inclusion/Exclusion criteria for the respective trial or to create your own shortlist of most frequently reviewed Inclusion/Exclusion criteria for the study.
Both of these lists can be printed by using the "printer" icon in the top right corner of the table.
We believe all sites should be able to afford StudyTeam, so we've guaranteed it.
Professional License
Sites can use StudyTeam without paying any fees. We provide StudyTeam licenses for your entire team, including access to the latest features, live training for new team members, and ongoing support by phone and email.This means that even if you learn about StudyTeam through a sponsor for a specific trial, you can use StudyTeam for all of your trials free of charge (and continue using it after that specific trial concludes).
Enterprise License
If your site needs custom features or integrations with your in-house technology systems, contact us. We may be able to help now or in the near future.
Why are Professional licenses free?
OneStudyTeam believes that every site deserves to have access to effective, user-friendly software. Your work makes clinical research possible, and helping you is how we achieve our mission. Therefore, our company is investing in your success -- for the long haul. We've made a commitment to make Professional licenses free for all sites.
Our Support Team will actively work with our Product and Development Teams to prioritize resolving bugs and addressing your feedback.
Provide feedback or report a bug in StudyTeam by creating a ticket here.
For feature and design requests you can also directly contact our Product Management Team:
Each patient added to a StudyTeam trial is given a Status which reflects that patient’s stage in the recruitment and screening pipeline.
There are 10 patient statuses to pick from:
Active Patients
One of the benefits of using StudyTeam with your sponsors is the ability to effortlessly share your recruitment efforts with them.
When a trial is linked to a sponsor they have the ability to view some of the information stored in your trial.
Sponsor are limited to what they can view in StudyTeam and Patient Identifiable Information will be automatically hidden from your sponsor.
The following article outlines what type of data your sponsor can access.
Currently, the ability to print reports is not a feature within StudyTeam, but it is on the horizon!
Until printing report is available, we have a way to help you when you need to print reports. The process involves taking screenshots which save to your computer as images and can be printed.
There are steps for both Mac and Windows users here.
When working in some areas in StudyTeam, such as the Patient Log, you may sometimes see this alert on text fields.
This is a friendly reminder not to enter patient identifying information into fields that your sponsor could have access to.
Trials in StudyTeam can be "connected" with your sponsor. When this happens, your site shares the progress of its recruitment efforts with your sponsor.
If the study has a pre-screening or screening/enrollment log, you can complete it electronically within StudyTeam. When the sponsor is connected, they can download it themselves without you needing to send them in.
If you are sharing your log with your sponsor would will see the following badge letting you know:
Due to a bug in older versions of Internet Explorer 11, sometimes patients can be added to StudyTeam but then not appear on the trial board. Another symptom of this bug is to restrict users from changing a patient's status on the trial board.
If you are experiencing this issue, there are two possible solutions:
Updating Internet Explorer 11 Settings
We implement rigorous security practices to keep all your data protected.
All of our systems and processes are at or above the standards of HIPAA and GDPR. Data is secure and encrypted in both transmission and at rest.
Our customers have vetted and approved of our compliance. In the past year alone, StudyTeam has passed security reviews by several hundred clinical research sites.
Contact us if you have any questions.
We maintain a strict firewall between your site’s patient information and all other users.
While StudyTeam can help you work with sponsors by automatically sending them data on your recruitment efforts, identified patient information is never shared with sponsors.
See what sponsors see here.
Back to the topIf you are interested in becoming a user and learning about StudyTeam's features, schedule an Introduction to StudyTeam.
You can add new users to your site by following these steps.
Trials in StudyTeam can be "connected" with your sponsor. When this happens, your site shares the progress of its recruitment efforts with your sponsor. Learn how a connected sponsor can save you time and improve your recruitment process here.
Back to the topMarkdown is a lightweight and easy-to-use way to format text when writing on the web. This formatting includes adding bolding, italics, headers, and images.
Currently, there are two places in StudyTeam you can use Markdown formatting:
Markdown works by adding symbols before and after sections of text, then once the text is saved the formatting will be displayed. For example, adding two asterisks before and after text will bold it the enclosed text. See a complete list of examples here.
Back to the topInstead of using a paper checklist for pre-screening patients, use a digital checklist within StudyTeam to help you stay organized and screen potential patients more efficiently!
Use the I/E checklist when determining eligibility of potential patients for specific trials. This could be used during a phone screening session with the patient, chart reviews, or other manners of pre-screening. Learn more here.
Back to the topAs StudyTeam for Sites is not a patient-facing application, communications directly with patients, including notification of sub-processing and obtaining consent, are managed by sites in accordance with their internal information handling practices. This is because sites are the data controller of their data and, therefore, each site follows its established notice and consent practices when doing any patient-facing work.