Clinical Trial Manager

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Clinical Trial Manager

Automate manual processes to cut costs and speed results

Designed with the versatility to accommodate your SOPs, Clinical Trial Manager and its modular design deliver unparalleled flexibility and ease of use. After a few hours of training, your study team will be setting up studies, defining protocols, managing user permissions—without the aid of IT staff. Whether managing multiple trials internally, or strategically outsourcing specific activities, TranSenda’s modular Clinical Trial Manager is the ideal clinical trial management system to enable your organization to become more productive and cost efficient.

As part of the TranSenda Central® system of integrated modules, all study data and protocols are extended and supported throughout complementary applications like TranSenda’s Clinical Payment Manager™ or into Clinical Trial Manager's business intelligence component, CTM Dashboard.

Total time saved by Clinical Trial Manager’s automated features can be hundreds of hours in a typical study.

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Clinical Trial Manager Key Benefits

• Decrease costs by automating manual processes and accomplishing more with less
• Increase productivity by using a single source for maintaining critical study data and documents, reducing the need for internal staff to input data
• Keep better track and control of clinical study sites and operations by using a web-based clinical trial management system designed by study professionals
• Improve teamwork using collaboration portals that provide secure  remote access to all study team members
• Versatile set up accommodates SOPs, allows custom alert notification, protocol deviation tracking and more

Clinical Trial Manager Key Features

• Study configuration wizard enables dynamic site initiation for either single or multi-sponsor users
• Robust scheduling functionality tracks and monitors patient visits and CRF receipts, can also set multi-mode alert schedules and triggers
• Context-intelligent navigation across standardized screens
• Integrated contact management and messaging
• Extensive tracking includes subject screening and enrollment; study visits; site monitoring; CRF page status; test article and  supply shipments; SAE disposition, action items and reconciliation; documents; correspondence and more
• Advanced record lookup capability
• Users can securely perform study-specific roles via flexible operational permissions
• System validation is facilitated through embedded features, test scripts and documentation