Clinical Trial Software for Contract Research Organizations

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Patient Management

CRO: When Collaboration is Key

Collaborating with partners, sponsors, and monitoring is always at the forefront for Contract Research Organization leaders. The CCTrialSuite uniquely empowers your CRO to increase site engagement, standardize site-level data collection, and streamline remote monitoring to ensure data quality for maximized trial success. CCeSource makes remote monitoring a breeze; now your CRO can reduce study delays and establish easy-to-use data capture workflows for your study sites.

Why CCTrialSuite for CROs?

Faster Enrollment

Flexible Configuration

Configured to successfully manage multiple trials at multiple locations.

Increased Accessibility

Effortless Remote Monitoring

Robust eCRF monitoring with standardized site workflows and simple monitor login access 24/7.

Streamlined Communication

Enhanced Communication

Provides transparent communication channels with your sponsors and partner sites.

Standardized Compliance

Project Management

Includes site-level study progress reports, multiple EDC interfaces, advanced regulatory document management, advanced eSource data capture and business intelligence reporting.

Enhanced Site Selection

Enhanced Site Selection

Leverage past site performance and other recorded data to develop high-quality lists of potential study sites in just a few minutes.


Real-Time Analytics

Quickly identify minor study progress issues at sites before they become major delays, generate complex study reports and access site-level info at any time for monitoring.

Clinical Trial Software for CROs

Clinical research management system for single sites and enterprises.

The industry’s most complete CTMS-EDC integration.

The industry’s most advanced patient payment application.

Text messaging solution designed to boost patient engagement and retention.

Capture source data in real time, enhance data quality and optimize site operations.

Efficient document management system for managing complex regulatory requirements.

The only electronic consenting system for sites that keeps patients engaged, ensures participant understanding, simplifies oversight and improves the overall consenting process.

What Contract Research Organizations Are Saying

New Horizons Clinical Research
Case Study

“CC CTMS allows us to track inbound calls in real time so we can understand which recruitment efforts are working, which ones aren’t, and then quickly reallocate funds and reach our goals.”

Case Study

“Now, CRS is a company with moving pieces that all work together. It has really made a huge change in our business.”

Resources for CROs

Blog Post
Ensure You Have Everything You Need for Remote Trial Visits Strong eClinical platforms, sponsor demands, regulatory process updates, and the current research environment have made decentralized trial management more accessible to clinical sites than ever. Remote monitoring – and its implications for how long and how costly a trial will ultimately be – is a […]

Revolutionize the way you conduct clinical research.

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