Clinical research teams often face fragmented workflows, slow recruitment, and high screen-fail rates. These challenges are amplified when referrals come from multiple sources and pre-screening is done without comprehensive checks before the patient reaches the site. The result is delayed trial timelines and added burden for coordinators, who must determine which patients are the best fit for enrollment, ideally with high confidence that those patients will remain engaged throughout the study.
The myTomorrows referral platform is designed to simplify and accelerate the pre-screening process. It centralizes all incoming referrals, whether from patients or caregivers themselves or from physicians, including specialists and community hospitals, into one unified system. This provides your site full visibility and control over referral activity, while reducing administrative overhead.
To improve both the volume and quality of referrals, the platform applies automated eligibility checks before they reach your site. These checks help ensure that incoming patients are more likely to meet your trial’s criteria, reducing screen-fail rates and saving valuable time for your team. While the system filters out clear mismatches, your site retains full control over final eligibility decisions, ensuring that clinical judgment remains central to enrollment.
By using a managed referral platform, your site can move from fragmented recruitment to a streamlined, compliant, and patient-friendly process. Your site will enroll faster, perform more confidently, and reach more patients and physicians, reducing screen failures and minimizing manual pre-screening time.
This article will explain how site teams can use the platform to track referrals, update custom trial information and use it to securely communicate with stakeholders. It will also cover off data privacy and compliance questions as well as explain additional support myTomorrows offers sites.
Getting started with the myTomorrows referral platform is quick and straightforward. Once registered, your site can begin receiving pre-screened referrals, access trial-specific tools, and collaborate with Patient Navigators, all within a secure, compliant environment.
Inform myTomorrows which trials you want to link to your account, and we will collaborate with the sponsor to activate them. Trials should be visible within 2 business days.
If your trial(s) aren’t visible within 2 business days, email medical-community@mytomorrows.com with the trial details.
You will have access to real-time updates, patient context, and ongoing support, helping you streamline recruitment and reduce administrative burden from day one.

To keep referrals accurate and aligned with your site’s current needs, you can post Trial alerts directly within the platform. These alerts let you share recruitment updates or referral requirements with referring physicians and Patient Navigators.
You can update or archive alerts anytime. All changes are versioned and visible to referrers, helping reduce mismatches and improve referral quality.
Please note: Keep alerts short, specific, and up to date to avoid unnecessary declines and ensure streamlined recruitment.

Once your trials are activated, you will begin receiving referrals directly through the platform. Each referral includes key patient context and is pre-screened based on your trial’s criteria, saving time and improving match quality.

The platform is designed to support secure, real-time collaboration between your site but also external stakeholder such as referring physicians, specialist, and sponsors.
This connected environment helps reduce delays, avoid miscommunication, and ensure that everyone involved in the referral process is working from the same, up-to-date information.
In certain programs, Patient Navigators are included as part of the site agreement to enhance patient engagement and streamline communication. When active, they serve as a vital link between patients, caregivers, referring physicians, and research coordinators, helping ensure everyone involved in the referral process is informed and aligned.
Navigator support may not be active at your sites initially. If your site is not yet connected to this service, referrals will still arrive with pre-screening context, and you can communicate directly with referring physicians (or other stakeholders) through the platform.
Data privacy and compliance are embedded into every step of the referral journey through a robust multi-consent flow. Whether initiated by a patient, physician, or caregiver, explicit consent is always obtained upfront, ensuring our patient-first principle remains central.
As a Clinical Research Team (CRT), you will initially access only de-identified data to assess eligibility. Personally identifiable information, including medical records and responses to key pre-screening questions—becomes available only if the patient, or their physician acting on their behalf, has provided consent.
All data is:
This enables allows you to manage recruitment workflows with confidence, knowing they align with the highest international standards: GDPR, HIPAA, ISO, SOC 2, and ICO registration.

We have a team dedicated to support our clinical site partners.
For questions, technical issues, or feedback related to referrals or platform functionality, please:
All inquiries are reviewed promptly to ensure timely resolution and to support the continuous improvement of the platform.
Below is a quick recap of the most common questions clinical sites ask. The following additional questions expand on specific platform features and site-level workflows.
Once you accept a referral, the patient’s contact details are revealed, and you can proceed with your site’s workflow. This may include scheduling a screening visit, requesting additional documentation, or initiating informed consent. Acceptance does not imply enrollment, it simply signals your intent to follow up.
Yes. If your site is temporarily unable to screen or enroll patients, you can update your recruitment status in the platform. This ensures referrals are paused and helps maintain transparency with referring entities.
Through our Matching API and integrated data tools, we help sponsors and CROs assess site feasibility based on therapeutic area, indication, geography, and historical referral data. This can position your site for future trial opportunities aligned with your expertise.
Sites have access to referral tracking dashboards, funnel insights, and performance metrics. Premium users receive enhanced analytics, including referral conversion rates, patient engagement data, and operational efficiency indicators.
By centralizing referrals, applying AI pre-screening, and enabling early eligibility insights, the platform helps sites focus on high-potential candidates and reduce unnecessary screening steps.
Referring entities can be onboarded to use the platform’s referral tools. Once authorized, they can securely pre-screen and submit referrals directly to your site, ensuring compliant and streamlined patient matching.
You can update your trial listing and site profile to include specific inclusion/exclusion criteria, preferred contact methods, and operational notes. This helps ensure referrals are better aligned with your site’s capabilities and expectations.
We offer:
About the author
Senior Community Development Manager at myTomorrows
Adrianne Rivard is the Senior Community Development Manager at myTomorrows, where she builds relationships and supports healthcare professionals at major neuromuscular and neurodegenerative disease centers across the US and Europe. She holds a bachelor’s degree in human biology with a specialization in Human Health and Disease from Indiana University Bloomington. Adrianne brings experience from Tempus AI, where she worked in clinical operations using AI-driven precision medicine to improve clinical trial matching and patient care, and from time as a Senior Surgical Pathology Technologist at Northwestern Medicine.
Adrianne Rivard 14 Nov 2025