Overview
SiteVault CTMS streamlines clinical trial management by giving study teams a centralized platform to manage protocols, track participant activity, and oversee study financials from start to finish. From pre-award budgeting and visit scheduling to post-award invoicing and payment reconciliation, SiteVault CTMS supports every phase of a study.
Built on the same platform trusted by 450+ sponsors and CROs, SiteVault CTMS reduces duplicate data entry and managing protocol milestones, saving sites time, effort, and unnecessary cost.
Benefits
Streamline Site Operations
Keep trials on schedule, manage study pipeline and monitor staff workloads and more with one centralized system designed to easily organize and track study details, staff and key milestones.
Scale Research Capacity
Expand trial capacity without increasing administrative overhead. With embedded, validated AI to automate specific manual tasks, SiteVault acts as a workforce multiplier so your teams can focus on patient care, and the critical thinking work they are trained for.
Eliminate Lost Revenue
Gain clear insight into earned and forecasted study revenue to make informed financial decisions with simple, customizable reports and dashboards. Capture and recognize all earned revenue with automated tracking of unbilled activities, unpaid invoices and invoice aging.
Improve Participant Experience
Get real-time visibility into patient status, visit management, and procedure completion to ensure nothing gets missed and every participant has a
smooth trial experience.
Minimize Duplicate Data Entry
Save time and reduce manual work with a CTMS that’s fully unified with your eSource, eISF and eConsent. Also designed to connect seamlessly
with sponsor and CRO systems, SiteVault is one connected core to manage your clinical trials.
For more information including key features download our product brief!
