Reach patients others miss.
A Raleigh-based standalone clinical trial site built on real community relationships, multi-TA execution experience, and the operational depth to start fast and deliver clean data. One team, directly accountable on every study.
We aggregate patient access across multiple trusted Triangle practices, spanning primary care, specialty, and community health, including practices serving largely minority and underinsured populations. Sponsors get the depth of a network with the responsiveness of a single owner-led site.
41
Providers across signed partner practices
~2,100
Patients seen weekly across the partners
~122k
Patient records across the partner network
Multi-TA
Coverage across primary care, specialty, and community health
Built to reach populations that drive enrollment diversity.
Patient records aggregated across formal practice agreements spanning primary care, orthopedics, psychiatry, and community health. Active EMR access across signed partner practices, searchable by diagnosis, medication, and demographics — giving sponsors a realistic pre-screen population before a study opens.
Multiple patient pools
Relationship-driven enrollment
In-house digital marketing
Active TAs supported by 59+ studies of prior team experience across Phase II and Phase III.
Operational Commitments
Fast. Clean. Accountable.
72hr
FEASIBILITY
Feasibility questionnaires and key protocol questions returned within 72 hours with realistic assumptions, not optimistic ones. Early flags on anything that could affect your study before you commit.
What to expect
Honest population estimates based on actual partner data. Competitive enrollment assessment with realistic screen-to-enroll projections. Protocol feasibility flags raised before you commit, not after.
48hr
CONTRACTS
Commercial cycles that do not slow start-up
Budget and contract responses within 48 hours. Direct access to the founders throughout, not a contracts department with a queue. We move at the pace you need.
What to expect
CEO directly accessible on budget negotiations. No layered approvals. Activation to first screen targeted within 30 days of IRB approval.
5 day
QUERIES
Data quality that does not require chasing
Query responses within 5 business days. Issues escalated within 24 hours. Robust SOPs and regulatory workflows in place before our first study opens, not assembled during it.
What to expect
Audit-ready documentation as standard. Protocol deviations reported proactively before monitor visits. Ongoing enrollment updates and site communication without sponsors having to ask.
“The people making commitments to sponsors are the same people responsible for delivery.”
COMMUNITY FIRST CLINICAL RESEARCH
Built for quality. Committed to lasting local impact.
Most sites you evaluate have been through at least one ownership change. The investigators who built patient trust are no longer running day-to-day operations. Financial professionals are.
| CFCR | PE Networks | IROs | |
|---|---|---|---|
| Trial operations | Standalone site | Varies | Inside clinic |
| Direct access | High — founders only | Varies | Varies |
| Patient pools | Multiple | Varies | One per site |
| Community trust | Structural reinvestment | Minimal | Existing patients |
| Geographic focus | North Carolina | Spread nationally | Spread nationally |
| Ownership | Real locals | VC / PE | VC / PE |
Experience across every side of the research ecosystem.
Our team has built sites, run studies, and sat across the table from sponsors.
We have managed the coordinators, timelines, budgets, and audits that determine whether a study succeeds.
We have delivered enrollment built on trust in underserved communities.
That perspective is built into every decision we make at CFCR.