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For sites that need participants

Your studies can reach people — without staffing a dedicated outreach role

“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.

What your coordinator actually sees

A review packet — not a score, not a quota

Study introductions and consented participant handoffs land as packets your team can accept, schedule, or close. Illustrative coordinator view.

CRC review packet

Consented introduction for an open protocol

Ready for study-team review
Consent
Recorded before any contact details moved
Region
ZIP3 on file — no full address in this view
Preferred channel
Phone or email, per the person
Your next step
Review inclusion/exclusion. Enroll only if you decide.

Corterve does not determine eligibility and does not promise enrollment.

What this takes off your plate

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.

People who may be new to research

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 a study is not the right next step

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.

A record you can stand behind

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.

Book an Exploratory Call

Tell us about your open studies. We will reply and take it from there.

Therapeutic areas your site can support.

When your site has capacity — not a community-engagement start date.

Do not send patient data

This channel is designated for strategic partnerships and feasibility inquiries. Do not submit patient-level data, Protected Health Information (PHI), or proprietary protocol datasets through this form. Use only non-sensitive business details here; we will follow up through approved channels if a secure exchange is needed.

How we handle information

Encrypted in transit and at rest. Shared with a study team only after consent. Read what we claim.

HIPAA-Aligned Architecture

Privacy-by-design practices aligned to HIPAA requirements. Code evidence — not a certification.

End-to-End Data Encryption

Patient data encrypted in transit and at rest across all platform surfaces.

Strict Consent-First Routing

No patient information is shared without explicit, informed consent.