A Study Is Starting
A new or upcoming study can introduce its own recruitment plan, patient communications, scheduling needs, and enrollment workflow.
Clinical Trial Enrollment Support
There’s More to Enrollment Than Finding Potential Participants.
Consent2Randomize can help research sites bring in potential participants, handle the follow-up and early enrollment work after someone shows interest, or both.
Your site decides what C2R handles for the study. That may include recruitment, intake, site-approved preliminary prescreening, follow-up, scheduling, documentation, and a clear handoff to your research team.
When C2R May Be Useful
Not every study needs outside enrollment support. But a new study, changing patient interest, or a shift in study activity can change what the enrollment work looks like.
Patient Interest Is Increasing
Referrals, sponsor programs, outreach, or recruitment can change the amount and timing of patient interest reaching the site.
The Enrollment Work Changes
Several active studies, a new protocol, or changing study requirements can change which enrollment tasks need attention and when.
What Can C2R Handle?
The scope can be built around the study and the way your site wants the work handled.
Finding Potential Participants
Patient recruitment when additional candidate flow is needed.
Responding and Following Up
Initial response, permitted follow-up, reminders, and keeping the current status clear.
Intake and Preliminary Prescreening
Collecting candidate-reported information and using site-approved preliminary questions.
Scheduling and Coordination
Helping coordinate permitted appointments and next steps.
Documentation and Handoff
Recording what has happened, what is still open, and what the research team needs when it takes over.
Your Research Team Stays in Control
C2R handles only the work your site has approved. Your research team remains responsible for formal screening, final eligibility decisions, informed consent, protocol oversight, medical decisions, and randomization.
Study-Specific Support
How It Works
C2R support is defined around the study. Your site decides what it wants help with, and C2R works within that agreed scope.
Choose the Study
Start with the active or upcoming study where enrollment support may be useful.
Define What C2R Will Handle
Agree on the part of recruitment or early enrollment work C2R will support.
Work From the Agreed Scope
C2R handles the agreed work and provides the documentation and handoff defined for the study.
Experience Behind the Approach
Built from hands-on research-site enrollment experience.
C2R draws on hands-on experience supporting research-site prescreening and pre-consent workflows across sponsor-funded clinical trials, including work involving AbbVie, Astellas, Amgen, Gilead Sciences, Janssen, Myovant, Novartis, Pfizer, Regeneron, Receptos, and more.
This describes prior site-level experience and does not imply direct sponsor engagement, current affiliation, or endorsement.
Review the experience behind the C2R approach →Tools & Resources
Tools for Examining Enrollment. Hands-On Support for Doing the Work.
C2R's resources help research sites examine enrollment workflow, economics, and readiness. The tools support the conversation. C2R can also take on agreed recruitment and early enrollment work for a specific study.
Have an Active or Upcoming Study?
Tell us how you expect recruitment and early enrollment to work for the study. We can look at where C2R may be useful and what your team wants to continue handling.
No PHI needed.