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Top 57 Clinical Trial Management Systems SaaS Companies in May 2026

As of May 2026, there are 57 SaaS companies in Clinical Trial Management Systems. They have combined revenues of $800.5M and employ 5K people. They have raised $866.2M and serve 2.3M customers combined.

Clinical Trial Management Systems (CTMS) are specialized software solutions designed to streamline the planning, management, and oversight of clinical trials. These systems help researchers and organizations to efficiently handle various trial processes, including participant recruitment, data collection, regulatory compliance, and reporting. CTMS are integral for ensuring that clinical studies are conducted effectively and adhere to industry standards. Primary use cases of CTMS include managing trial workflows, tracking patient visits, monitoring data integrity, and facilitating communication among stakeholders. Key features often involve data management capabilities, dashboards for real-time insights, and automation of administrative tasks such as scheduling and regulatory filings. Users of CTMS typically include clinical research organizations (CROs), pharmaceutical companies, and academic institutions engaged in clinical research.

Companies
57
Revenue
$800.5M
Funding
$866.2M
Employees
5K

Filters

Sorting: Highest -> Lowest

Filters

Top Clinical Trial Management Systems Companies

Showing 10 of 12 companies ranked by annual revenue.

1
The Concinnity Company

Nashville, Tennessee, United States

Cloud Concinnity® is an integrated platform that centralizes, simplifies and automates control of data, communications, process management & reporting, while unlocking the value of big data. Our platform provides the most functional and comprehensive clinical trial oversight software on the market: a single, secure hub where all meetings, documents and processes can be centralized, automated, monitored and generate a complete audit trail. Cloud Concinnity enables developers of new therapies to bring their treatments to market faster, at a lower cost all while reducing risk to Sponsors, Clinical Research Organizations (CROs) and patients.

Revenue
$990K
Customers
-
Year founded
-
Funding
-
Team size
9
Growth
-
2
Healex

Cologne, North Rhine-Westphalia, Germany

Healex bridges the gap between clinical research and clinical care with seamless structured clinical data solutions to accelerate and improve clinical research and trial management. Healex develops and licenses SaaS, on-premises enterprise software and web applications for seamless clinical data management designed to help hospitals, research organisations and pharmaceutical companies with speeding up and executing multi-site clinical trials. Healex provides fully integrated platforms for rapid integration of high-quality, real-time structured clinical data across multiple sites facilitating the move to a FHIR based healthcare industry. By supporting international, open medical data standards such as the FHIR data standard, Healex solutions can be seamlessly integrated into existing hospital systems and electronic patient records, making it easier for patients, clinics and health insurance companies to use clinical data in a wide range of applications. Healex software is proven by over 6300 researchers at 340 hospitals and across 3000+ studies.

Revenue
$990K
Customers
-
Year founded
2019
Funding
-
Team size
9
Growth
-
3
ancora.ai

Zürich, Zurich, Switzerland

Ancora. ai is an AI -driven, digital clinical trial navigation platform connecting cancer patients to clinical trials.

Revenue
$990K
Customers
-
Year founded
2017
Funding
-
Team size
9
Growth
-
4
Intrinsic Clinical Systems

United States

Intrinsic Clinical Systems is the result of decades of pharmaceutical, clinical trial, project management, and operations experience. We’ve made it our mission to design simple, easy-to-use software for the pharmaceutical industry – software that feels more like today’s intuitive apps than yesterday’s clunky desktop applications. If you’re looking for a solution that’s more scalable than Excel but not so complicated as all the legacy applications out there, Intrinsic is for you. Having worked with traditional clinical trial management systems, feasibility tools, resource planning applications, and time tracking tools, we’ve felt the pain that comes with the needless features and huge price tags of those systems. We’ve heard the industry’s requests for cloud-based tools that are affordable, easy to use, and don’t require an IT department to manage. And our solutions can be implemented in a matter of days, not months or years like other systems on the market.

Revenue
$880K
Customers
-
Year founded
2014
Funding
-
Team size
8
Growth
-
5
HealthKey

Austin, Texas, United States

AI-powered Patient Identification for Clinical Trials

Revenue
$880K
Customers
-
Year founded
2023
Funding
-
Team size
8
Growth
-
6
ShareCRF - EDC Software

United States

We get our clients to optimise their clinical trials processes. Our aim is to simplify the duties associated to these processes and for that reason we offer the simplest way to deal with them. We listen to our clients and learn their needs to provide specific solutions using our EDC platforms. To find out how we do it, and how we could help your organisation, schedule an introductory call with us: https://www.sharecrf.com/demo

Revenue
$880K
Customers
-
Year founded
2000
Funding
-
Team size
8
Growth
-
7
MolecularMatch

Houston, Texas, United States

MolecularMatch, Inc. is a Houston, Texas-based clinical informatics SaaS company founded in 2014 out of MD Anderson Cancer Center. The company was founded on the vision of using tumor molecular profiling, and outcomes from previously-treated patients, to provide the best personalized treatment for current patients. MolecularMatch delivers personalized, evidence-based therapeutic guidance and clinical trials matched to each patient. Customers include genetic labs, health information systems, biopharma, hospitals, and cancer centers.

Revenue
$880K
Customers
-
Year founded
2014
Funding
-
Team size
8
Growth
-
8
Sensivo

Norra Djurgården, Sweden

Sensivo is a company that provides data management solutions for clinical research.

Revenue
$594.8K
Customers
-
Year founded
2019
Funding
-
Team size
2
Growth
105.73%
9
Mosio for Research

Seattle, Washington, United States

WHAT WE DO: Mosio enables clinical research teams to improve patient adherence, communications, and data collection on mobile's most popular channel: text messaging. If you're finding, like other researchers, that phone calls and email isn't getting the job done, it's time for text messaging, which can be automated, personalized, and easily integrates with third party clinical trials software like EDC, CTMS, ePRO, or eCOA. Study sponsors, CROs, Principal Investigators, and research teams use Mosio to improve patient engagement, retention, and data collection efforts with interactive mobile messaging. Our software makes research teams more efficient in how they communicate with study participants through messaging automation and interactive elements delivered to participant mobile phones. WHO WE HELP: Clinical Trial Sponsors (Pharma and Biotech) Cancer Centers and Clinical Research Organizations NIH-Funded Studies Clinical Trial Managers, Clinical Operations Managers/Direct

Revenue
$339.8K
Customers
-
Year founded
2007
Funding
-
Team size
9
Growth
36.12%
10
MaganaMed GmbH

United States

Intuitive and secure software for clinical trials: from electronic data capture (EDC) with eCRFs (electronic case report forms) to ePRO/eCOA/eDiary. Compliant with GCP, FDA CFR part 11, GDPR (german: DSGVO), ISO 14155. Meets all requirements of FDA, BfArM, ethic committees, MDR, IVD-R, and notified bodies. All kinds of studies possible and validated: academic research, clinical research, studies for product registrations, PMCF studies, pharma trials. The modular system allows you to configure the software to your specific needs - you only pay what you need. Made in Germany!

Revenue
$330K
Customers
-
Year founded
2017
Funding
-
Team size
3
Growth
-

Inclusion Criteria

- The software must provide end-to-end management capabilities for clinical trials. - It should facilitate regulatory compliance and ensure adherence to trial protocols. - The system must offer data management and reporting functionalities. - It should include features for tracking patient recruitment and participation. - Must support seamless communication among research staff and stakeholders. - Not just for data entry; must also automate administrative tasks and workflows.