The AI orchestration platform for clinical trials

AI That
Shows Its Work

Transform a clinical trial protocol into one unified Study Definition that orchestrates study builds, data, and workflows across the clinical technology ecosystem.

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One Protocol
Unified Study Definition
AI Orchestration
Every Clinical System
Unified Data
✓Continuous Insight
Today
PROTOCOL Clinical Trial Protocol Application groups parse the protocol and interpret the protocol independently. EDC EDC Study Build Independently configured 01 DB RTSM RTSM Study Build Independently configured ABC 01 CTMS CTMS Study Build Independently configured DB TBL Safety Safety Study Build Independently configured DOC 01 Payments Payments Study Build Independently configured 01 TBL Labs Labs Study Build Independently configured DB 01 8–12 WEEKS Manual study build Fragmented data, minimally integrated. DATA MANAGER Constant management of data Sporadic reporting CLINICAL STUDY BUILD — TODAY PROTOCOL → INDEPENDENT TEAMS → INDEPENDENT STUDY BUILDS → FRAGMENTED DATA → MANUAL MANAGEMENT 8–12 WEEKS · Constant Management of Data · Sporadic Reporting
Protocol → Independent Teams → Independent Study Builds → Fragmented Data → Manual Management
With Synthia
PROTOCOL Clinical Trial Protocol Interpret once. Deploy everywhere. SYNTHIA Unified Study Definition EDC RTSM CTMS Safety Payments Labs 1 DAY Automated study build EDC Study Build Generated automatically RTSM Study Build Generated automatically CTMS Study Build Generated automatically Safety Study Build Generated automatically Payments Study Build Generated automatically Labs Study Build Generated automatically One dataset. Every system in sync. UNIFIED DATA Standardized study data 01 DB ABC 01 DB TBL DOC 01 01 TBL DB 01 LIVE STUDY LEAD Continuous data synchronization Real-time reporting CLINICAL STUDY BUILD — WITH SYNTHIA PROTOCOL → SYNTHIA → UNIFIED STUDY DEFINITION → AUTOMATED BUILDS → UNIFIED DATA → REAL-TIME REPORTING 1 Day · One Study Definition · Automated Builds · Continuous Data Synchronization · Real-Time Reporting
Protocol → Synthia → Unified Study Definition → Automated Study Builds → Unified Data → Real-Time Reporting
The Synthia Platform

AI Orchestration

Synthia creates a unified digital Study Definition from the clinical trial protocol and uses AI orchestration to drive consistent study builds across the clinical technology ecosystem.

See Synthia on your next study

Walk through how a protocol becomes a unified Study Definition — and how that definition orchestrates every connected system.

Platform

One Study Definition. Every Clinical System.

Synthia sits above the clinical technology stack. It converts the protocol into a unified digital Study Definition, then orchestrates study builds, data, and workflows across the systems you already use.

SourceClinical Trial Protocol
↓
SynthiaUnified Study Definition
↓
CapabilityAI Orchestration
↓
EDC
RTSM
CTMS
eCOA
Safety
Labs
Payments
eTMF
↓
OutputUnified Study Data
↓
OutcomeContinuous Reporting & Insights
What Synthia accomplishes

Orchestration, not another application to implement

Synthia does not replace EDC, RTSM, CTMS, or safety systems. It gives every connected application the same digital study to execute against.

01

Define the study once

The protocol becomes a unified digital Study Definition — the common foundation for configuration, data, and change.

02

Orchestrate every system

Study builds are generated consistently across the clinical technology ecosystem from that single definition.

03

Stay in sync

Amendments, data, and reporting remain aligned because every system is working from the same study, not a separate interpretation of it.

See how orchestration fits your stack

A working session on your protocol, your vendors, and the systems you already run.

Solutions by Role

One foundation. Value across the ecosystem.

Synthia creates value across the clinical trial ecosystem by giving sponsors, CROs, and technology vendors a common digital foundation for study execution.

For eClinical Vendors

Become AI-ready without asking customers to switch platforms

Accelerate Implementation

Move customers from study requirements to configured applications faster.

Reduce Professional Services

Automate repetitive study-build and configuration activities.

Increase Customer Satisfaction

Reduce implementation timelines and improve consistency.

Become AI-Ready

Connect existing applications to an AI orchestration layer without requiring customers to replace their technology.

For CROs

Standardize delivery across every sponsor stack

Deploy Studies Faster

Move from protocol to operational study systems faster.

Reduce Manual Configuration

Automate repetitive study-build activities across multiple applications.

Standardize Delivery

Establish consistent study definitions, terminology, configurations, and workflows across sponsors and studies.

For Sponsors

Shorten startup. Standardize globally.

Shorten Startup

Reduce the time between protocol completion and operational system readiness.

Reduce Cost

Reduce repetitive interpretation, configuration, and reconciliation activities.

Improve Quality

Maintain consistency across systems using a common Study Definition.

Standardize Studies Globally

Create a common digital foundation across studies, CROs, vendors, and geographies.

Partners & Ecosystem

Built for the ecosystem you already run

Synthia is designed to work across the clinical research ecosystem, connecting the technologies and organizations responsible for executing modern clinical trials.

Names and logos identify companies and platforms in the clinical research landscape. They do not, by themselves, indicate a customer, partner, or technology-integration relationship.

Build with the stack you have

Talk with us about connecting Synthia to the platforms, CROs, and sponsor environments you already use.

Resources

Ideas Shaping the Future of Clinical Trials

Perspectives on AI, digital protocols, clinical technology, study orchestration, and the transformation of clinical trial execution.

An industry knowledge center — not a product blog. The work here is about where clinical technology is going, and the architecture required to get there.

About Synthia

Our Mission

To transform how clinical studies are defined, built, executed, and managed through AI orchestration.

Synthia converts every clinical protocol into a unified digital Study Definition and uses that definition to orchestrate study builds, data, and workflows across the clinical technology ecosystem. We exist so sponsors, CROs, and technology vendors can define the study once — and orchestrate it everywhere — without replacing the systems they already run.

Leadership

Built by experienced eClinical operators

Ron Burns

Ron Burns

CEO & Co-Founder

Serial entrepreneur. Founded ProtonMedia, launched multiple enterprise platforms at Bioclinica, and drove AI-enabled clinical trial strategies at Biofourmis. Deep eClinical build and scale experience.

Douglas Cory

Douglas Cory

CTO & Co-Founder

Founder of Phoenix Data Systems, acquired by Bioclinica. Oversaw global engineering teams at Bioclinica and Clario, delivering regulatory-grade, cloud-based platforms across the full eClinical stack.

Richard Murg

Richard Murg

CCO & Co-Founder

Led global sales at Bioclinica, Biofourmis, Veranex, Clario, and MedNet. Consistently delivered double-digit revenue growth and secured enterprise pharma partnerships at scale.

Advisory Board

Guided by leaders who have shaped clinical development, technology, and life sciences

Jason Attanucci

Jason Attanucci

Synthia Advisory Board

Commercial leader with over two decades in eClinical and clinical trial technology. Most recently Chief Commercial Officer at Image Analysis Group; previously Vice President and General Manager, Life Sciences at Deep 6 AI, with additional senior commercial leadership roles at Medidata Solutions and Bioclinica. Holds a B.S. in Molecular Biology from the University of Pittsburgh and studied Immunology at the University of Pittsburgh School of Medicine.

Dr. John Hubbard

Dr. John Hubbard

Synthia Advisory Board

Ph.D. in cardiovascular physiology and Fellow of the American College of Clinical Pharmacology. Most recently President and CEO of Bioclinica; previously Senior Vice President and Worldwide Head of Development Operations at Pfizer and Group President of ICON's Clinical Research Division. Currently Chairman of the Board at Signant Health.

Nancy Maher

Nancy Maher

Synthia Advisory Board

CIO, CTO, and CDO with executive roles at Merck, Schering-Plough, Gilead Sciences, Teva, Allergan, Kyowa Kirin, and Ergomed. Brings deep expertise across the life sciences value chain, with a strong focus on AI, data, and the regulated systems that support clinical development, commercial execution, and regulatory outcomes.

Careers

Join Us

We work hard. We work together. And we're changing the way clinical trials are built.

Synthia brings together experienced clinical technology leaders, engineers, AI specialists, and industry innovators with one goal: fundamentally improve the way clinical studies are designed, built, and executed.

Culture

How we work

High performance

We set a high bar for craft, speed, and follow-through — because clinical operations cannot wait on unfinished work.

Collaboration

We work as one team across product, engineering, and the industry operators who have lived study startup.

Innovation

We apply AI where it changes study execution, not where it merely looks advanced.

Accountability

We own outcomes in a regulated environment: quality, traceability, and decisions that stand up to scrutiny.

Clinical impact

The work matters because faster, more consistent study builds help research reach patients sooner.

Entrepreneurial thinking

We are building the next architecture of clinical research — and we expect everyone here to help shape it.

Open Positions

Build the orchestration layer for clinical trials

No open roles posted right now

We're always interested in meeting exceptional people who believe clinical research can work better.

Contact

Request a Demo

Tell us a little about your study or your organization, and we'll show you how Synthia orchestrates it end to end.

Thank you! We'll be in touch within 24 hours.
02

Platform walkthrough

A 30-minute working session on your protocol and systems.

03

For eClinical vendors

Ask about connecting your application to Synthia orchestration.

04

For CROs & Sponsors

Ask about a pilot study with your next protocol.