Clinical Trial Enrollment Operations
Enrollment Workflow Support After Patient Referrals Come In
Consent2Randomize provides hands-on early enrollment operations support after a referral or patient inquiry reaches the research site and before informed consent.
Hands-on enrollment support for research sites
C2R can support candidate intake, candidate-reported information collection, site-approved preliminary prescreening, permitted follow-up, appointment readiness, documentation, escalation, and structured handoff. The research site retains clinical judgment, eligibility, informed consent, screening, protocol oversight, and randomization.
Featured operational resources
Review the pre-consent workflow
Use the Prescreening vs. Screening guide to review the boundary between preliminary operational support and formal site screening.