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Corterve

For sites that need studies

Study finding for sites with capacity and no BD person

“We have clinic capacity and no one whose job is finding new studies.”

Lean sites rarely staff business development. We look for studies that may match your experience and capacity, then introduce you. You remain the investigator. Sponsors still select sites.

Independent and small research sites with unused capacity and no one whose job is finding studies.

Book an Exploratory Call
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.

Site coordinator inbox

Protocol conversation ready for review

Awaiting investigator decision
Indication
As stated in your capacity profile
Setting
Outpatient research visit
What we did
Found a study that may fit your experience and capacity
What we did not do
Award the site or commit your investigators

Sponsors and CROs still decide the award. You remain the investigator.

What changes for you

  • You are no longer the person hunting for the next protocol after clinic.
  • Rapid 48-hour feasibility questionnaire turnaround using your certified site capability profile.
  • Objective CTA budget benchmarking to recover fair market value, startup costs, and institutional overhead.
  • Remote startup document preparation so your team walks into SIV prepared. Sponsors and CROs still decide the award.
  • You stay the investigator. We take on the finding and startup coordination.

Also need people for the studies you already have? See the participant solution.

Book an Exploratory Call

Tell us about your site, capacity, and therapeutic areas. We will talk about whether study finding is a fit.

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.