Clinical researchSites and networks

Clinical research, from patient access to site growth.

Our teams help research sites and networks find patients, win studies, and run them well. We also help physician practices join research the right way.

89%

of investigative sites activate and begin enrolling.

Tufts CSDD
<0.2%

of physicians and nurses actively refer patients to trials.

Tufts CSDD survey
40%

longer study startup timelines than a decade ago.

Tufts CSDD
$55.7K

approximate daily cost of running a Phase III trial.

Tufts CSDD, 2024

How investigative sites perform against enrollment targets

Across nearly 16,000 sites in 151 Phase II and III trials, almost half of the sites selected either enrolled nobody or fell short.

11%Enroll no patients
37%Under-enroll
39%Meet the target
13%Exceed the target

Source: Tufts Center for the Study of Drug Development

From screened to completed

Across therapeutic areas, about half of all patients screened go on to complete a trial, which is why the top of the funnel has to be full.

Source: Tufts Center for the Study of Drug Development

In the field

Find the patients. Win the studies. Run them well.

Four teams working from one plan across the life of a site.

Clinician and patient discussing treatment options
Patient access and enrollment

Recruitment that starts in the community.

The patients a site needs are already seeing a physician somewhere nearby. Our enrollment team builds the referral relationships, outreach, and pre-screening that bring them in.

  1. 01
    Referral networksCommunity practices connected to the studies a site is running.
  2. 02
    Community outreachPrograms built around the populations a site serves.
  3. 03
    Pre-screeningQualified candidates handed to coordinators, not raw leads.
What we do

Four teams across the life of a site.

Patient access, business development, operations, and investigator networks, working from the same plan.

Patient access and enrollment

Recruitment built around the community a site serves, from outreach and referral networks to pre-screening and retention.

  • Recruitment strategy
  • Community outreach
  • Pre-screening

Business development

Positioning sites with sponsors and CROs, answering feasibility well, and building a pipeline of studies that fits the site.

  • Sponsors and CROs
  • Feasibility
  • Study pipeline

Site operations

Startup, staffing, training, and SOPs that hold up to monitoring visits and keep studies moving on timeline.

  • Startup
  • Staffing
  • Quality

Investigator networks

Principal and sub-investigators sourced from our provider network and matched to what a site is enrolling.

  • PI sourcing
  • Referral partners
  • Embedded sites

What an idle site costs

A study that runs 30 months at a site that enrolls a single patient.

$40Kto activate the site
$90Kat $3,000 a month to manage
$130Kfor one enrolled patient

Source: Phesi, based on typical site activation and management costs

Where a new site's first year goes

The milestones our teams plan against, from the first feasibility question to steady enrollment.

FeasibilityPopulation, therapeutic mix, payer profile, staffingWeeks 1 to 4
BuildCredentialing, regulatory documents, coordinator hiringMonths 1 to 3
ConnectionSponsor and CRO introductions, feasibility packagesMonths 2 to 5
ActivationFirst study awarded, site initiation visitMonths 4 to 8
EnrollmentReferral network live, first patients inMonths 6 to 12

Timelines are typical ranges and vary by therapeutic area and sponsor.

Partnership models

How practices and sites work together.

Four models, from a simple referral relationship to a full acquisition, each scoped to what both sides can support.

01

Referral partnership

Community practices refer qualified patients into a site's active studies.

02

Investigator engagement

Physicians join a site as principal or sub-investigators on studies matched to their specialty.

03

Embedded site

Research operations run inside an existing practice, staffed and supported by the site partner.

04

Acquisition

Sites and practices identified, introduced, and prepared for acquisition by growing networks.

Researcher at a microscope
The patients a site needs are already in a waiting room nearby.Northstra Health clinical research
Clinicians reviewing study documents together
Site operations

Operations that hold up to a monitoring visit.

Startup, staffing, training, and SOPs that keep studies on timeline and keep sponsors coming back.

  1. 01
    StartupRegulatory packets, budgets, and contracts moved on schedule.
  2. 02
    Staffing and trainingCoordinators hired and trained to the protocol.
  3. 03
    QualitySOPs and documentation ready for monitoring and inspection.
Insights

From our clinical research practice.

How we think about enrollment and site economics.

Physician and patient in a consultation
Clinical research

Enrollment is a community problem before it is a marketing problem.

Very few physicians and nurses ever refer a patient to a trial. Sites that enroll well build referral relationships with the practices their patients already trust.

Scientist examining samples at a microscope
Clinical research

Every idle site has a cost.

A site that never enrolls still has to be activated, monitored, and managed for the life of the study. Feasibility is the cheapest place to find that out.

Grow the site you are building.

Whether the need is patients, studies, investigators, or operations, start with a conversation.