Outreach when you have no one assigned to it
Small sites rarely have a person whose job is finding participants. We help with that outreach so your coordinators are not starting from a blank page. They still screen, consent, schedule, and decide.
For sites that need participants
“We have studies and no one whose job is finding participants for them.”
Your open studies can reach people without you staffing a dedicated outreach role. We help people discover your studies and, with their consent, introduce them to your team. You keep seeing patients. Your study team decides who joins.
Lean sites with awarded studies and no dedicated recruitment staff.
Study introductions and consented participant handoffs land as packets your team can accept, schedule, or close. Illustrative coordinator view.
CRC review packet
Corterve does not determine eligibility and does not promise enrollment.
Small sites rarely have a person whose job is finding participants. We help with that outreach so your coordinators are not starting from a blank page. They still screen, consent, schedule, and decide.
We look for people who have not been recycled through digital ads, so your team can talk with a person — not a purchased list. Trial-naive is a sourcing aim, not a guarantee about every introduction.
If someone is not right for a study, that is the study team’s call. They may still ask about care at your practice — only if they want that, and only with a separate consent. A screen-fail is not a practice conversion.
Each consented interaction is documented in a way a study team can review. We do not decide eligibility and we do not promise enrollment.
Also need help finding studies for the site? See the study solution.
Tell us about your open studies. We will reply and take it from there.
Encrypted in transit and at rest. Shared with a study team only after consent. Read what we claim.
Privacy-by-design practices aligned to HIPAA requirements. Code evidence — not a certification.
Patient data encrypted in transit and at rest across all platform surfaces.
No patient information is shared without explicit, informed consent.