Simplifying Clinical Trial Management With One Platform For All Your Data
At Remarque Systems, our mission is simple: provide a single, easy, and effective platform to manage all your clinical trial data. We deliver this through an intuitive and flexible platform that:
- Consolidates all your data from different sources in real-time
- Delivers end-to-end visibility and oversight with data-driven analysis, monitoring, and risk assessment
- Drives better-informed decisions with clear and conclusive analytics, reports, and visualizations
The result: Consolidating your data on one powerful platform brings process optimization, increased visibility, rapid communications, and improved quality to your clinical trials.
The History of Remarque Systems
In 2015, clinical trial data was managed by large and expensive technology; and a significant amount of manual work was done by clinical research staff. We believed there was a better way.
Taking a ground-up approach, we set out to develop a system that allows study stakeholders to get actionable access to trial data. We merged expertise in science, operations, and technology to establish effective processes and got to work focusing on risk-based monitoring and its dependence on data.
First, we tackled the standardization of non-standardized data. This data was spread across systems, often buried in email or a spreadsheet, frequently managed by a CRO — and extremely important to the sponsors.
Then, we created our platform. Our parameters were strict:
- No technical skills required to manage
- Works with legacy systems and evolving technology
- Data integration would be simple and seamless
- Analytics would be a core function
- User interfaces would be intuitive
- Supports tracking, managing, and audit trailing
We built it. We launched. And then we kept working, expanding the platform to meet the evolving needs of our customers.
Today, Remarque Systems supports risk-based quality management. We provide real-time cleaning of redundant data, early identification of safety signals, and support for Data and Safety Monitoring Board meetings with clear graphic visualizations that illustrate progress towards study endpoints.
We’re not stopping here. We continue to evolve the Remarque Systems platform in partnership with our customers, helping you find the most effective way to manage your clinical trial data.
We bring together leading experts in data analytics, machine learning, data visualization, science, and clinical trial management.
We partner with our customers to ensure that every step of the process is seamless, intuitive, and valuable.
We continually expand and enhance the platform to support the expanded use cases that our customers request.
Senior Management Team
Joe is a data guy at heart. He’s also an eternal optimist who believes in creating and using technology for a purpose. With over 25 years in technology most of it spent in Healthcare and Lifesciences he has led the implementation of many platforms. His key skill lies in translating business challenges into innovative technology solutions in a regulated environment.
Crystal brings expertise from 15 years of experience in clinical trial operations and management to her leadership role with Remarque Systems’ team of software subject matter experts. With a background in research and engineering, she now has over six years of clinical trial software management experience.
With over 20 years in the pharmaceutical industry, Wade’s focus is on software development and enterprise architecture. As a key leader on Remarque Systems’ technology team, his skills include business analysis, data warehousing, software development, integration and more.
With over 25 years of experience as an Enterprise Architect and Information Consultant at Eli Lilly and Quintiles, Dan became a leading member of the Remarque Systems technology team. He brings a deep technology skill set that includes data integration, software development, data management and more.
With over 7 years of applying machine learning to healthcare data, Basheer is Remarque Systems’ lead data scientist. He previously worked at IQVIA (Quintiles), where he built predictive models and interactive visualizations for analytics projects. He holds a Ph.D in Computer Science from The University of Louisville and has authored several peer-reviewed papers.
After 26 years at Eli Lilly as a Statistician, Susan joined Remarque Systems as a Product Owner with a focus on data quality. She is passionate about leveraging technology and data to solve problems in the clinical development space. She holds an MS in Statistics from Iowa State University.