medical professionals working

Accelerating the discovery of treatments that work.

Every trial we conduct, every patient we enroll, every data point we capture brings us closer to answers that change lives.
WHO WE ARE

Research That Finds the Cure

Clinicians Guild exists at the intersection of clinical practice and scientific discovery.

We conduct FDA-regulated, IRB-approved clinical trials with the rigor of academic research centers and the operational efficiency of specialized research sites.

Our investigators are practicing physicians who bring real-world patient populations into controlled research environments where breakthrough therapies are tested, validated, and advanced toward approval.

** This is not about healthcare delivery. This is about healthcare advancement.

people lifting hands
OUR COMMITMENT

We don't promise cures.

We promise the rigorous scientific work necessary to discover them.

On-Time Delivery

Trials completed on time and on budget.

Patient Enrollment

Patient populations successfully enrolled.

Regulatory Data

Data quality that meets regulatory standards.

Proven Outcomes

Approved treatments that trace back to our research sites.

Phase Advancement

Therapies advanced from Phase II to Phase III

Phase
Advancement

Therapies advanced from Phase II to Phase III

Phase
Advancement

Therapies advanced from Phase II to Phase III
The CG Model

You run and oversee everything...

Whilst the Clinicians Guild team does 90 percent of the work.

Turn-key Operations

Everything required to run research is managed end-to-end within your practice.

Turn-key Operations

Everything required to run research is managed end-to-end within your practice.

Turn-key Operations

Everything required to run research is managed end-to-end within your practice.

Revenue Enhancement

Sponsor-funded trials deliver predictable revenue without upfront financial risk.

Revenue Enhancement

Sponsor-funded trials deliver predictable revenue without upfront financial risk.

Revenue Enhancement

Sponsor-funded trials deliver predictable revenue without upfront financial risk.

Rapid Start-Up

Established workflows enable studies to launch quickly and efficiently.

Rapid Start-Up

Established workflows enable studies to launch quickly and efficiently.

Rapid Start-Up

Established workflows enable studies to launch quickly and efficiently.

Reduced Research Burden

Operational and regulatory tasks are handled externally.

Reduced Research Burden

Operational and regulatory tasks are handled externally.

Reduced Research Burden

Operational and regulatory tasks are handled externally.

Shorter Study Timelines

Streamlined processes reduce delays across the study lifecycle.

Shorter Study Timelines

Streamlined processes reduce delays across the study lifecycle.

Shorter Study Timelines

Streamlined processes reduce delays across the study lifecycle.

Improved Patient Care

Patients access innovative therapies within trusted, physician-led care settings.

Improved Patient Care

Patients access innovative therapies within trusted, physician-led care settings.

Improved Patient Care

Patients access innovative therapies within trusted, physician-led care settings.
OUR RESEARCH MISSION

Finding the Cure Requires Three Things

As a PI, your responsibilities are clearly defined and protected, allowing you to remain the clinical leader.

Rigorous Scientific Standards

Every trial we activate meets FDA regulatory requirements and follows Good Clinical Practice guidelines.

Diverse Patient Populations

We bring clinical trials to community settings where patient demographics represent the populations who will ultimately use these treatments.

Operational Excellence at Scale

Every day a promising therapy sits in trials is a day patients wait for better treatment options.

girl in blue jacket holding red and silver ring
WHAT WE DO

Operational Enablement

Our model removes operational barriers that prevent qualified physicians from participating in research, enabling us to:
Activate sites rapidly in geographies where sponsors need patient access.
Enroll diverse patient populations that reflect real-world treatment scenarios.
Maintain protocol compliance through dedicated research coordinators.
Generate high-quality data that regulators and sponsors trust.
Accelerate trial timelines through efficient operations and proven processes.
man in white dress shirt wearing black sunglasses
man in white dress shirt wearing black sunglasses
man in white dress shirt wearing black sunglasses

Current Therapeutic Areas

Hematology
Gastroenterology
Cardiology & Metabolic Disease
Neurology
Infectious Disease
Immunology
Pulmonary & Critical Care
Rheumatology
Hematology
Infectious Disease
Gastroenterology
Immunology
Cardiology & Metabolic Disease
Pulmonary & Critical Care
Neurology
Rheumatology
Clinical Value Delivered

Trial Phases

Our focus is exclusively on Phase 2, Phase 3, and Phase 4 clinical research—where studies can run efficiently in outpatient settings, with high-quality execution and strong patient access.

Phase 2

Proof in Patients

Early efficacy and dose validation in a defined patient population.

Tight protocols, frequent checkpoints, high operational rigor.

Phase 3

Confirmation - Scale +

Larger populations to confirm outcomes across broader, more diverse cohorts.

Heavy focus on enrollment reliability, compliance, and consistency across sites.

Phase 4

Real-World Evidence

Post-approval studies that measure long-term safety, outcomes, and real-world performance.

Often supports label expansion, comparative studies, and ongoing safety monitoring.

Explore research participation.

A simple eligibility review helps determine if participation is right for you.
Join the Guild
FAQ
FAQ

Your Questions. Answered.

Your Questions. Answered.

Contact us if you have any other questions.
Contact us if you have any other questions.

Do I need prior research experience to participate?

Do I need prior research experience to participate?

Do I need prior research experience to participate?

Will clinical research disrupt my existing practice or patient care?

Will clinical research disrupt my existing practice or patient care?

Will clinical research disrupt my existing practice or patient care?

Who is responsible for regulatory compliance and audits?

Who is responsible for regulatory compliance and audits?

Who is responsible for regulatory compliance and audits?

Is there any upfront cost or financial risk to my practice?

Is there any upfront cost or financial risk to my practice?

Is there any upfront cost or financial risk to my practice?

orange bubbles art
Contact Us
Contact Us

A Curated Network.

A Curated Network.

This isn't about exclusivity for its own sake. It's about maintaining the scientific rigor and operational precision that sponsors demand and patients deserve.

Every investigator in our network represents Guild's reputation to regulatory authorities, institutional review boards, and pharmaceutical partners.

We select carefully because the research matters.
This isn't about exclusivity for its own sake. It's about maintaining the scientific rigor and operational precision that sponsors demand and patients deserve.

Every investigator in our network represents Guild's reputation to regulatory authorities, institutional review boards, and pharmaceutical partners.

We select carefully because the research matters.
For Sponsor Partnerships
For Doctors Partnerships

A clinical research institution dedicated to conducting FDA-regulated trials that advance medical science and contribute to the discovery of tomorrow's cures.

Clinicians Guild © 2025

A clinical research institution dedicated to conducting FDA-regulated trials that advance medical science and contribute to the discovery of tomorrow's cures.

Clinicians Guild © 2025