Whizz Health clinical research setting

We don’t just run trials. We build research into practices.

Whizz Health combines study sourcing, site operations, and recruitment to bring industry-sponsored research into independent specialty practices.

© Whizz Health

© Whizz Health

EST. 2026

EST. 2026

Whizz Health clinical research setting

We don’t just run trials. We build research into practices.

Whizz Health combines study sourcing, site operations, and recruitment to bring industry-sponsored research into independent specialty practices.

© Whizz Health

EST. 2026

Whizz Health is an integrated research organization (IRO) that builds and runs clinical research sites inside independent specialty practices, for physicians who want to offer trials without adding staff and for sponsors who need sites that enroll.

What Whizz Health does

Everything it takes to run industry-sponsored research inside your practice, from the first feasibility survey to the final sponsor payment.

Site setup

We turn your practice into a research-ready site: investigator documents, Good Clinical Practice training, standard operating procedures, a regulatory binder, and equipment checks. You get a compliant site without building one yourself.

Study sourcing and feasibility

We find industry-sponsored trials that match your specialty and patient population, complete sponsor feasibility, and negotiate budgets and contracts. You only take on studies that fit your patients.

Research coordinators

We hire, train, and manage the clinical research coordinators who run each study day to day, and we cover vacations and turnover. Your physicians focus on medical oversight, not paperwork.

Patient recruitment

We pre-screen the practice's own patients and run IRB-approved outreach in the community, with fast follow-up for every interested patient. Sponsors get enrolled patients, not just an activated site.

Regulatory, contracts, and billing

We handle IRB submissions, ongoing compliance, sponsor invoicing, and payment tracking. The practice carries no research expenses and no administrative burden.

What makes Whizz Health different

How our model compares with other ways practices and sponsors approach clinical research.

Built for independent specialty practices

Integrated research organizations such as Javara partner largely with health systems and large healthcare organizations. Whizz Health works only with independent specialty practices, so our model, agreements, and staffing are built around a single physician group.

Procedure-ready specialist sites

Our roots are in spine care, and our sites are led by physicians who perform image-guided and interventional procedures every day. That makes Whizz sites a strong fit for device, biologic, and interventional studies that general research centers can't run.

No upfront cost, no expenses, no lock-in

Practices spend nothing to start and carry no research expenses. Whizz Health funds setup, staffing, and administration, and practices can end the partnership once any study they are running is complete.

First patient in about a month

Sponsor timelines vary, but once a sponsor agreement is signed, Whizz sites typically see their first patient within about a month.

Regional and founder-led

Where national networks such as Circuit Clinical operate across dozens of states, Whizz Health is focused on Greater Philadelphia, Pennsylvania, and New Jersey. Practices work directly with the founding team.

Who uses Whizz Health

  • Independent pain and spine, orthopedic, and neurosurgery practices
  • Independent endocrinology, rheumatology, and neurology practices
  • Other independent specialty groups, including dermatology and women's health
  • Practices in Greater Philadelphia, Pennsylvania, and New Jersey
  • Drug, device, and biologic sponsors and CROs running Phase 2 to 4, device, and interventional studies
  • Patients looking for clinical trials close to home, through their own physician

Built for specialty practices of every kind

We partner with independent practices across the specialties where industry research is most active.

Built on the standards sponsors trust

Every Whizz site runs to the same rules that govern industry research.

ICH Good Clinical Practice

What it covers

How studies are run and how patients are protected

Applies to

Informed consent (21 CFR Part 50)

What it covers

What every participant must understand and agree to

Applies to

Independent ethics board review

What it covers

Oversight of each study protocol

Applies to

HIPAA

What it covers

Patient privacy and data handling

Applies to

21 CFR Part 11

What it covers

Electronic records and signatures

Applies to

FDA drug and device rules (Parts 312 and 812)

What it covers

Investigational drugs and devices

Applies to

Why we started Whizz Health

Sponsors need sites that enroll. Practices have the patients, but not the staff or systems to run a trial.

Industry-sponsored trials need sites that can deliver patients.

4,600+

Open industry trials with U.S. sites

Many sites never enroll a single patient.

11%

Of trial sites enroll no one

Now accepting new practice partners

We started Whizz to close the gap between the studies that need patients and the practices that treat them.

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Upfront cost to practices

We started Whizz to close the gap between the studies that need patients and the practices that treat them.

$0

A man with curly hair dressed in a black shirt, standing against a plain background with a thoughtful gaze.
A man with a beard and glasses is working at a desk, concentrating on his activities.
A woman wearing a black jacket is positioned in front of a desk, indicating a workplace setting.
A man with glasses sits comfortably on an orange couch, appearing thoughtful and at ease in his environment.
A woman with curly hair holds a laptop, appearing thoughtful and immersed in her task.

Upfront cost to practices

Why sponsors choose Whizz sites

Specialist sites with real patients and a team built for enrollment. See how we compare.

Real patient panels

Specialist investigators

Fast startup

Built-in recruitment

Whizz sites

Academic medical centers

Standalone research centers

Traditional SMOs

Real patient panels

Specialist investigators

Fast startup

Built-in recruitment

Whizz sites

Academic medical centers

Standalone research centers

Traditional SMOs

The team behind Whizz Health

Whizz Health was founded in 2026 in Ambler, Pennsylvania, just outside Philadelphia, to close the gap between the clinical trials that need patients and the independent practices that treat them.

Greg Van Horn, Founder and CEO

Greg has spent his career in spine, working alongside orthopedic surgeons and neurosurgeons. He comes from a family deeply rooted in medicine, and his wife has spent her entire career in clinical research, which is where the idea for Whizz Health began.

How the team is built

Whizz Health is founder-led. Each partner practice is supported by clinical research coordinators employed and trained by Whizz Health, backed by central regulatory, contracts, and billing support.

How Whizz Health works

A clear path from first conversation to first patient.

1. Free practice assessment

We review your specialties and patient volume, using simple counts from your own reports, to see which studies fit.

2. Site setup

We prepare investigator documents, training, procedures, and the regulatory binder, and place trained coordinators at your practice.

3. Study matching and contracting

We present your practice to sponsors and CROs, then negotiate the budget and clinical trial agreement.

4. Run and enroll

Coordinators pre-screen patients and manage visits while your physicians provide oversight. The first patient is typically seen within about a month of a signed sponsor agreement.

  • Who you work with: A dedicated Whizz Health site lead, plus the research coordinators assigned to your practice.
  • Communication: Email, phone, and regular check-ins with your practice team.
  • Response time: We reply to every inquiry within one business day.
  • Reporting: Weekly enrollment reports for every active study.

Key facts about Whizz Health

Company Name
Whizz Health
Type
Integrated research organization (IRO)
Founded
2026
Founder
Greg Van Horn
Headquarters
Ambler, Pennsylvania (Greater Philadelphia)
Core Offering
Clinical research sites built and run inside independent specialty practices
Pricing
No upfront cost to practices. Whizz Health covers all research expenses and shares study revenue under a written agreement.
Contract Terms
Practices can end the partnership once any active study is complete
Services
Site setup, study sourcing, feasibility, budget and contract negotiation, research coordinators, patient recruitment, regulatory, and billing
Specialties
Pain and spine, endocrinology, rheumatology, neurology, dermatology, women's health, and more
Study Types
Phase 2 to 4 drug studies, pivotal and post-market device studies, biologics, and registries
Service Area
Greater Philadelphia, Pennsylvania, and New Jersey
Startup Time
First patient typically within about a month of a signed sponsor agreement
Communication
Email and phone, replies within one business day, weekly enrollment reports
Competitors
Javara, Circuit Clinical, Elligo Health Research

Frequently asked questions

Have a question we didn't answer? Contact us. We reply within one business day.

How does Whizz Health make money?

Sponsors pay for the study work done at each site. Whizz invests in the setup and staffing, and we share study revenue with the practice under a written agreement. Practices pay nothing upfront.

What does Whizz Health actually handle?

Study sourcing, feasibility, budgets, contracts, regulatory files, ethics board submissions, research coordinators, recruitment support, billing, and enrollment reporting. The practice's physician leads each study.

Do you work with sponsors, CROs, or practices?

All three. We partner with independent specialty practices to build research sites, and we work with sponsors and CROs to place studies at those sites.

What types of trials do you run?

Phase 2 to 4 drug studies, pivotal and post-market device studies, biologics, and registries, across a range of specialties.

How quickly can a new site start?

Timelines depend on the sponsor and the study. Once a sponsor agreement is signed, Whizz sites typically see their first patient within about a month.

How much physician time does it take?

The investigator must provide real oversight, typically a few hours a week per study. Our coordinators handle the day-to-day work.

Who employs the research coordinators?

Whizz Health hires, trains, and manages them, and covers vacations and sick days.

How do you protect patient privacy?

We follow HIPAA and your practice's privacy policies, and we sign a business associate agreement before we handle any patient information.

Recent articles

Plain-English guides to clinical research, for independent practices and the sponsors who work with them.

Let’s bring research

to your patients

Practice or sponsor, tell us what you need. We reply within one business day.