About us.

SiteCentric CTMS+ platform was built to address needs of a major US-based multi-specialty clinical research site network. It was built from over 25 years of experience in running clinical trials.

To date, no CTMS system on the market comes close to SiteCentric capabilities and built-in workflow efficiencies.

Let’s Meet!

Principal Investigator interacting with SiteCentric CTMS+

Core Modules

The power of our solution comes from its integration. All modules “talk” to each other seamlessly sharing data to optimize workflows, reduce knowledge silos and increase efficiency, quality while lowering cost.

CTMS+

Easy to use clinical trials management software for clinical trials centered around clinicians and investigators. Each screen is meticulously designed around their needs. Less clutter, more efficiency.

Compliance, Regulatory and Quality Assurance

Manage your regulatory milestones and quality from a single system. Allow easy remote monitoring with the use if our eISF. Connected to the CTMS to stop easily preventable deviations.

Patient Recruiting and Advertising

One-of-a-kind recruitment efforts management tool to keep track of your study budgets and ROI’s. Seamlessly tied in with the CTMS for real-time performance data.

Business Development

Business Development is a major part of your organization’s success. Instead of using expensive Salesforce, image an integrated solution to fit into your workflows.

Billing and Revenue Management

Track your revenues, costs and advertising expenditures. Forecast revenues with a click of a mouse and generate invoices to sponsors and CRO with ease. Don’t leave potential revenue on the table because it is too hard to track; this fully integrated module has visibility into all SiteCentric CTMS+ modules!

eISF , eSource, eConsent & Remote Monitoring

Effortlessly communicate, access project plans, and make payments through our intuitive online platform.

eSource and eConsent Integration
eISF – Investigator Site File
eSource – Electronic Case Report Forms
eICF – Electronic Informed Consent

Remote monitorin g is included in both eISF, eSource, and eICF modules.

3000+

Studies Completed

The US-based site network that has developed SiteCentric completed over 3000 trials over the last 25+ years. All that expertise and experience is built into SiteCentric.

100+

FDA Approved Drugs

Over 100 compounds have secured FDA approval including large studies like those part of Operation Warpspeed that were supported by SiteCentric.

45+

FDA Inspections

Over the 25+ years, over 45 FDA inspections have been performed. All for high enrollment and not for cause. Many of them were supported by SiteCentric.

The People behind the scene

Meet our team

A collective of research site experience, innovative minds and spirited individuals, committed to developing a best-in-class platform to improve site operations and efficiency.