
Specialities
Emmes CRO possess experience across a broad range of therapeutic areas, with specializations in Vaccines and Infectious Disease, Ophthalmology, Clinical Neuroscience, Rare Disease, Cell and Gene Therapy and Government.
A Global, Full-Service Clinical Research Organization

Advancing human health with scientific rigor and integrity
Therapeutic Area Expertise
Digital First
Welcome to Emmes, a full-service clinical research organization (CRO) dedicated to helping biopharmaceutical, government, non-profit, and academic partners achieve their development and human-health goals.
We advance programs faster, more efficiently, and with higher quality through the end-to-end use of technology and data-driven science.

Emmes CRO possess experience across a broad range of therapeutic areas, with specializations in Vaccines and Infectious Disease, Ophthalmology, Clinical Neuroscience, Rare Disease, Cell and Gene Therapy and Government.

VaxTrials is Emmes CRO's vaccine and infectious disease center of excellence.
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Emmes CRO is a global leader in ophthalmology research, spanning retinal, corneal, and vision-restoration trials.
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Emmes CRO supports advanced cell and gene therapy programs, from early-phase studies through long-term follow-up.
Read moreEmmes CRO brings deep expertise to rare and orphan disease programs, navigating small patient populations and complex endpoints with care.
Government
For nearly 50 years, Emmes has partnered with U.S. government agencies to advance public health and scientific discovery.

From biostatistics to data management, our integrated clinical services span the full trial lifecycle — delivered with scientific rigor and operational excellence.
High Quality, Efficient, Biostatistical Support
Biostatistical support is essential to the design and execution of all phases of high-quality clinical trials. Our biostatisticians and clinical research scientists work hand in hand with sponsors and research teams — from study planning through final reporting.
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Accurate, Compliant, Audit-Ready Data
Our data management teams deliver clean, compliant, and analysis-ready datasets using validated systems and standardized processes that accelerate timelines without compromising quality.
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Emmes offers a robust suite of services for your Phase I-IV clinical trials, registries, observational studies and other clinical research.
Join us where collaboration between scientists, clinicians, biostatisticians, data scientists, and IT experts is producing the highest quality results.
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Clinical trial site management is a critical aspect of your trial’s success.
As your clinical trial and site management partner, we go to great lengths to support your sites and their patients.
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Helping you Navigate Regulatory Pathways
Emmes can help you navigate the investigational new drug, device and biologics regulatory pathways toward a successful product launch.
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To deliver life-changing medical advancements, the clinical research you put into global drug development requires dedicated and detailed management of clinical trial safety risks and high quality of medical monitoring.
As your partner in enabling patient safety and managing enrolled patients safely through the duration of your study, we can provide a forward-thinking approach and a coherent safety data plan.
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At Emmes Group, we collaborate closely with sponsors and research teams to deliver high-quality, data-driven clinical solutions. Connect with our experts to discuss how we can support your next clinical program.
Our clients enable us to make significant impact on pharmaceutical research and human health
98%
Client Retention
1,981
Longest Client
32,000
Clinical Trial Sites
30M+
eCRF Pages
The impact of this work is profound—providing a scientifically validated approach to slowing the progression of AMD, and improving quality of life for millions of patients worldwide.