CROs
The Opportunity
CROs have many responsibilities, ranging from site and vendor selection and management, to trial execution. There are many challenges to the timeliness and cost effectiveness of clinical trials rising from the lack of systemic, consistent workflow collaboration and information sharing across clinical research entities. Further, sites are tasked with efficient patient recruitment, study execution, regulatory compliance, management of study finances and communication – all while providing the best patient care, ensuring patient safety, and gathering accurate clinical data. Tools that improve workflow, facilitate communication, and provide metrics to track and demonstrate performance, are needed to streamline operations, reduce delays, and improve economic return.
Our Solutions
Clinical Conductor clinical trial management systems and tools handle the complete enterprise workflow, from business development, to patient databases, recruiting, scheduling, workload planning, finances, clinical data, and complete oversight and reporting. In addition to providing the workflow backbone, our CTMS integrates best-in-class tools and expertise, like electronic data capture and automated patient stipend payment, at natural points in the clinical trial process. Recognizing that little information technology exists to enable collaborative workflow and information sharing, we worked with CRO and site partners to develop our enterprise system. The result is improved financial performance, ready proof points, fewer project delays, and streamlined communications.
Our Products
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