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About ClearPoint

A proven partner
in clinical research.

ClearPoint Clinical Research Advisory was built on one belief: that both sponsors who need results and sites that deliver them deserve an expert, committed partner, one who stays engaged for the long haul.

What sets us apart
Precision
Every study match is backed by rigorous evaluation: no guesswork, no wrong fits.
Partnership
We remain fully engaged from startup through closeout, not just at the point of placement.
Performance
We set clear goals, track milestones, and are accountable to your outcomes, not just the process.
"We find the right fit.
Then we make sure you succeed."

ClearPoint was built on a simple premise: the most important thing we can do isn't just to make a match. It's to make the right one, then remain committed to your success at every step that follows. We are with you from the first conversation to final closeout.

100%
GCP compliant, every site, every visit
End-to-End
Support from site assessment through database lock
Precision
Matching based on protocol, population & capacity
Always
Engaged: an active partner, not a placement service
What guides us

Three values.
One commitment.

I
Precision

The right match,
every time.

Every recommendation we make is informed by a thorough evaluation of the protocol and the site, covering therapeutic area, patient population, operational capacity, and investigator track record. Precision means no guesswork, no wrong-fit placements, and no wasted time for anyone involved.

II
Partnership

In it with you,
for the long haul.

We build lasting relationships, not transactional engagements. Whether you're a sponsor meeting an enrollment deadline or a site navigating your first regulatory audit, our team is fully invested in your success, and we stay that way from the first site assessment through final closeout.

III
Performance

Accountable to
your outcomes.

At the end of the day, results are what matter. We set clear goals, track milestones, and actively intervene when performance falls short. Our team is accountable to your outcomes, not just the process of supporting them. We measure our success by yours.

Our home market

Deeply rooted in
South Florida research.

South Florida is one of the most vibrant and diverse clinical research markets in the United States, and ClearPoint is built to leverage every advantage it offers. Our deep local knowledge and vetted site network give sponsors and sites alike a meaningful competitive edge.

Unmatched patient diversity
South Florida's uniquely diverse population supports representative enrollment across a wide range of therapeutic areas and patient demographics, a critical advantage for your trial.
Deep local expertise
We know this market because we work in it every day: the sites, the patient communities, the healthcare infrastructure, and the regulatory landscape.
A thriving research ecosystem
From its large and growing retirement-age population to its diverse working-age community, South Florida supports enrollment across oncology, cardiology, CNS, metabolic, and infectious disease indications.
Our site network

Vetted for performance.
Matched with precision.

Every site in our network is evaluated for investigator experience, operational infrastructure, regulatory track record, and enrollment history before we make a single match. When we recommend a site, it's because we've done the work, and we're confident in the fit.

Evaluation criteria
Investigator experience & therapeutic expertise
Infrastructure
Operational capacity & research facility readiness
Compliance track record
GCP adherence history & regulatory inspection outcomes
Enrollment performance
Historical enrollment rates & patient retention data
How we work

Your journey with
ClearPoint.

Our five-step engagement model ensures consistent, expert support for every sponsor, every site, every trial. From first conversation to final closeout, you'll always know what comes next.

01
Site Assessment
We evaluate your site's strengths and capacity, or your protocol requirements as a sponsor, before making any recommendations
02
Study Matching
Precision alignment between protocol and site: therapeutic area, population, enrollment targets, and operational fit
03
Startup Support
Budgeting, GCP training, source document development, and regulatory guidance to set your trial up for success
04
Active Execution
Recruitment support, monitoring visits, compliance oversight, and active problem-solving throughout the trial
05
Ongoing Advisory
Dedicated consultation and advisory support from initial startup through final closeout and database lock
"We remain fully engaged from startup through closeout,
ensuring your site meets every goal, every milestone,
and every protocol requirement."
ClearPoint Clinical Research Advisory
Join the ClearPoint network

Partner with a team that's
as invested as you are.

Join the sponsors, CROs, and clinical sites across South Florida that trust ClearPoint to guide their research success, from the very first conversation through final closeout.

Start the Conversation
ClearPoint Clinical Research Advisory