Bring the future of medicine to your patients today!

By partnering with CCT Research as an Investigator, you get a ready-to-go solution for easily adding clinical research to your practice.

You get a dedicated research team, high-tech equipment, and a proven system embedded right into your office at no cost to you.

Offer your patients the most advanced treatments and increase your profits while becoming a leader in your industry. Let's build the future of healthcare together.

Partner Perspective

“Over 25 years of Research, I have learned that I prefer working with CCT Research. They provide the resources to get contracts with the sponsors, negotiate payments, staff to help me conduct the studies, and reassure all the data is prepared and submitted correctly. Trials run smoothly and our results meet the sponsor's goals. CCT has been a desirable clinical research company to work with.”
Dr. Fiel image
– Tom Fiel, D.O. Fiel Family and Sports Medicine and Team Physician of the Phoenix Suns

Intro to CCT Research

Network of research sites

  • 28 locations and growing across the US
  • Provider specialties: Family Medicine, Neurology, & Dermatology
  • Conducting Phase II – IV clinical trials across multiple specialties including vaccine trials
  • We partner with sponsors/CROs to bring novel treatments to patients locally

Faster Trials Fueled by Patient Access to Clinical Research

  • CCT is the second largest enroller, worldwide, in an AstraZeneca COVID Vaccine Trial
  • We embed our sites directly into physician’s offices to give patients direct access to clinical trials
  • Employ recruitment and partnership strategies to drive an expanding pool of patients in physician’s offices
  • Patients receive care they otherwise may not through a physician

Experienced Team & Research Staff

  • 150+ contracted providers
  • 150+ CCT full-time employees
  • 15+ years of industry experience across all operational leads

Our Network

CCT site map in united states

We’ve built an integrated (and growing) site network with the capabilities and resources to support the entire study cycle from pre-activation to study close.

Our focus is on Family medicine, Dermatology, Neurology, and Sports Medicine.

25
Embedded Sites
3
Dedicated Sites
2
ACO Partners
See our locations

Site Case Study

First year operationalizing one of our Utah sites

May 2020

Initial Meeting
Initial conversation with physician about joining CCT Research Network

July 2020

Contracts Signed
Fully finalized legal contracts to begin research

September 2020

First Study Awarded
Study officially awarded by sponsor/CRO

October 2020

Staffed & First Revenue
CCT Team Onboarded:  Site Manager, Clinical Research Coordinator, Research Assistant. Initial revenue realized.

November 2020

First Patient In
First research patient seen by CCT staff inside physician’s office

January 2021

Revenue to PI
$*****
(These revenue details shared in initial meeting)

July 2021

Revenue to PI
$******
(These revenue details shared in initial meeting)
May 2020
Initial Meeting
Initial conversation with physician about joining CCT Research Network

May 2020 // Initial Meeting

• Initial conversation with physician about joining CCT Research Network

July 2020 // Contracts Signed

• Fully finalized legal contracts to begin research

September 2020 // First Study Award (Month two)

• Study officially awarded by sponsor/CRO

October 2020 // Staffed & First Revenue (Month Three)

• CCT Team Onboarded:  Site Manager, Clinical Research Coordinator, Research Assistant. Initial revenue realized.

November 2020 // First Patient in (Month Four)

• First research patient seen by CCT staff inside physician’s office

January 2021 // Revenue to PI (Month Six)

• (These revenue details shared in initial meeting)

July 2021 // Revenue to PI (Month Twelve)

• (These revenue details shared in initial meeting)

Site Case Study
Operationalizing one of our Utah Sites

May 2020
Initial Meeting
Initial conversation with physician about joining CCT Research Network
July 2020
Contracts Signed
Fully finalized legal contracts to begin research
September 2020
First Study Award
Study officially awarded by sponsor/CRO
October 2020
Staffed & First Revenue
CCT Team Onboarded:  Site Manager, Clinical Research Coordinator, Research Assistant. Initial revenue realized.
November 2020
First Patient In
First research patient seen by CCT staff inside physician’s office
January 2021
Revenue to PI
These revenue details shared in initial meeting.
July 2021
Revenue to PI
These revenue details shared in initial meeting.

Why Join Our Network?

male doctor shaking senior male patient's hand
  • Business Development for your site. We bring trials to YOU!
  • We provide & pay for the necessary research staff to conduct each trial
  • We help identify and enroll patients into each study
  • We provide training for PI’s, Sub I’s and site staff
  • We provide educational materials for practices to discuss alternative options with their patients
  • Outside recruitment drives new patients to your practice
  • Equipment is purchased and set up by CCT
  • We take care of all Regulatory, QA/QC, Budget/Contract, IRB Submissions and many other processes so you don't have to!

Recent Study Achievements

stat: CCT Ranked number two globally for Covid Vaccine
Stat: 75% of our covid sites were top 10 enrollers on the study
stat: CCT Ranked number ONE enroller for Covid Vaccine
These achievements are more than just numbers. They equal a tremendous impact on patients, their families, physicians, and sponsors. Each trial can benefit millions of people now, plus help future generations to come.

Centralized Research Management

We provide everything you need to conduct research without the stress of managing trials.
Staffing Strategy
The CCT Operations team ensures proper staffing according to study complexity: Principal Investigator, Sub-Investigator, Clinical Research Coordinators, Research Assistants
Data & Tech
We provide all sites with a Clinical Trial Management System (CTMS) & centralized data management
Patient Recruiting
We handle recruitment from current site patient population and bring new patients into your practice through various marketing and outreach methods
Business Development
Manage sponsor relationships and sourcing new trials for all sites
e-SOURCE
Central team translates sponsor protocol into electronic visit schedule and documentation requirements
QA & e-Regulatory
Monitors performance, documentation, and other study processes from activation to study close-out
Budget & Contract
One budget, one contract per study for all sites

Keep Your Independence

woman

Your private practice can thrive among the hospital system giants!

We understand the financial difficulties private practitioners may face competing with the larger hospital systems.

By partnering with CCT Research, you’ll have another avenue to provide patient care and increase revenue directly into your practice.

Startup Timeframe

Estimated weeks for each step. Total setup time ranges from 5-18 weeks.
1. Initial conversations
1-3 weeks
2. Site qualification visits
3. Contracting process
4. First study award
1-2 weeks
1-3 weeks
2-10 weeks
In just a few weeks, you could add a profitable and rewarding income stream to your business!

Our Research Partners

AZTherapies
Abbott
Abbvie
Alkahest
Allergan
Astrazeneca
Axsome
Center for Derm
Cipla
GSK
Home Instead
Lilly
Merck
Mimedx
Moderna
Novartis
Novavax
Otsuka
Pfizer
Regeneron

Frequently Asked Questions

Who is a Principal Investigator (PI) and Sub-Investigator and what are their responsibilities?

The PI is one of the communities’ physicians and is the primary individual in charge of the clinical trial. The PI is ultimately responsible for the overall conduct of the trial and all personnel involved in the study. There is generally only one PI per site. 

The Sub I is a provider (MD, DO, NP or PA) who performs study related exams. Often times a trial will have multiple Sub I’s involved. 

Are physicians compensated for their involvement in a clinical trial?


Yes! While physicians are not paid an hourly rate for their time, they are compensated at fair market value rates for the services provided in each trial. 

Who takes on the liability and risk?

The pharmaceutical sponsor indemnifies the site, the principal and sub investigators and CCT. You will need to notify your malpractice carrier, but it shouldn’t impact your premiums. 

Will a patient be paid to participate in the clinical trial or is there a cost to participate?

Compensation for participants is unique with each clinical trial and each sponsoring partner. This is a question that should be discussed with the researcher when considering participating in a clinical trial. The experimental compound as well as tests and procedures associated with the trial are usually provided at no cost to the participant. In most cases, the cost of routine tests and procedures—not associated with the trial—are the responsibility of the participant, or the participant’s insurance carrier. 

Do we bill a patient’s insurance?

No! Everything related to a clinical trial will be paid by the pharmaceutical company. The patient will be responsible for the cost of routine medical care outside of protocol-required care. 

Can a participant leave a clinical trial at any point?

Yes. A participant can leave a clinical trial at any time. The participant should let the research team know when withdrawing from the trial and the reasons for leaving the study. 

Why partner with CCT Research?


By partnering with CCT we simplify the process of clinical research. We eliminate the hassle of staffing, business development and all back end operations. On top of this, we are focused on trials that fit the patient populations of our physicians sites. Because we create an infrastructure within the facilities, patients are more comfortable to participate in a research trial. 

Whether you're starting from the beginning or want to accelerate your research program, CCT is your partner that'll help you grow while easing the hurdles of research. Schedule a call with us to get a custom analysis and see how our partnership could benefit you.

Next Steps

One
After a pre-qualification call to learn about your site and answer your questions, we'll evaluate your practice for the right experience and patient population to be a successful research site.
Two
If your site qualifies, next, we get contracts in place and embed our research program, equipment, and a full-time coordinator into your site.
Three
Once we are set up, we begin marketing your site immediately for upcoming studies.
Schedule a Call

or Send us a Message

Or contact Josh Rindt,
Director of New Site Development
725-238-3380