clinicalconductor.comClinical Conductor - Clinical Trial Management System (CTMS)

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Get a Quote View All Services Solutions for Need Clinical Trial Management Clinical Data Management Research Administration Study Startup Site Support and Engagement Secure Document Exchange Decentralized Clinical Trials Oncology Research Early Phase Research Research Site Cloud Solutions for Sites Enterprise Institution CTMS Health System/Network/Site CTMS Electronic Consenting System eSource and Electronic Data Capture eRegulatory Management System Research ROI Reporting Automated Participant Payments Life Sciences Cloud Solutions for Sponsors/CROs Clinical Research Experience Technology Center for IRB Intelligence Insights for Feasibility IRB Document Sharing Not Sure Where To Start? 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Request a Demo TRUSTED BY CLINICAL RESEARCH LEADERS This was only achievable using a CTMS; manual reconciliation would have been prohibitive and likely not worth the ROI, so using Clinical Conductor was the only way for us to recover funds. Michelle Smith Research Business Analyst Ascension Healthcare Download the Case Study$100K Recovered In Unbilled Payments Why Clinical Conductor? Streamline Enrollment Use patient recruitment and enrollment tools to optimize your recruitment tasks, track progress in detail, and reach more participants in less time. Boost Profitability Run your research as a business with budgeting, billing, and reporting tools designed specifically for clinical research sites. Enhance Visibility Utilize advanced reporting and analytics to help measure your success, optimize operational workflows, and gain visibility into finances. Improve Participant Engagement Leverage add-on modules to easily reach your participants, reduce no- shows, and facilitate engagement throughout the study. Connect Your Technology Integrate with Advarra eReg or eSource + EDC, or use Clinical Conductor’s API to connect with other platforms throughout your organization. Securing Your Data with a Next-Generation Cloud Platform We are committed to the safety and security of your data, delivering technology solutions in an easy-to-use, fully managed cloud environment. We have received ISO 27001:2013 and SOC 2 Type 2 certification for our technology solutions, ensuring our products, services, and processes meet stringent requirements to enhance security and compliance. Advarra Security Advarra Cloud Enhance the Patient Experience Optional remote workflow enablement, communication, and payment modules to help you keep patients engaged and improve their overall trial experience. Two-way text messaging designed specifically for sites to maximize recruiting and reach enrollment goals, while dramatically increasing retention with HIPAA compliant, trackable messaging and reminders to participants in any location. Learn moreA HIPAA-compliant, patient-centric virtual meeting solution designed specifically for clinical research. Built into Clinical Conductor, CCVideo allows you to expand recruitment efforts and complete visits remotely with encrypted video sessions. Learn moreA secure patient payment system that revolutionizes the speed of payments with real-time reimbursements to prepaid debit cards, reducing fraud risk, reducing cost, and providing full oversight directly within Clinical Conductor. Learn moreAccess the Premier Research Community Advarra welcomes Clinical Conductor customers to a robust network of the nation’s leading clinical research professionals sharing best practices and addressing current challenges. The Onsemble Community allows researchers to collaborate with colleagues while shaping the industry and the technologies they use every day. By working together, we can all move clinical research forward. Learn More Connect Your Clinical Research Technology Clinical Conductor is seamlessly integrated with Advarra’s eReg and eSource + EDC platforms. Leverage these turnkey integrations to save staff time and improve data quality and compliance across your organization. Save money, improve efficiency, and enhance regulatory compliance across your organization with a 21 CFR Part 11-compliant system designed to adapt to regulatory management and eConsent workflows for any size research site. Learn moreEnable your staff to easily capture and manage data, facilitate remote workflows, and eliminate duplicative processes, all in a 21 CFR Part 11-compliant eSource + EDC system integrated with your clinical trial management system Learn moreScroll to Top Subscribe to our monthly email Receive updates monthly about webinars for CEUs, white papers, podcasts, and more. Subscribe Advancing Clinical Research: Safer, Smarter, Faster ™ Copyright © 2024 Advarra. All Rights Reserved. Privacy Policy Terms of Use Cookie Policy Advarra LinkedIn Advarra Facebook Advarra...