Technology
Technology-Powered Clinical Development
Flexibility and Expertise to Drive Faster, Smarter Decisions—Across Every Study Phase and Touchpoint
At Premier Research, we combine advanced clinical technology with deep operational expertise to streamline study execution and deliver high-quality, submission-ready data—on time and with confidence.
Whether you need full-service clinical development or targeted functional support, our technology ecosystem empowers your team and ours to stay aligned, informed, and agile—from study start-up through close-out.
Unified CTMS for Seamless Study Management
Premier Research leverages a configurable, role-based CTMS built on the Remarque platform, designed to bring all study data, documentation, and analytics into one centralized solution. This includes project management, financial oversight, site monitoring, and operational analytics—all within a single, integrated environment.
Project teams stay grounded in daily operations, executive leaders maintain strategic oversight, and sponsors benefit from transparent, real-time access to study progress. This streamlined approach enhances collaboration, supports faster decision-making, and helps keep trials on track—even when unexpected challenges arise.
Tech-Enabled Risk-Based Quality Management (RBQM)
Our RBQM framework, also powered by the Remarque platform, combines centralized monitoring, risk mitigation, and clinical analytics in one cohesive system. Aligned with ICH E6(R3) guidance, this solution empowers teams to act on real-time insights, identify issues early, and maintain quality while reducing the overhead of traditional monitoring models.
Our platform offers a unified system that enhances collaboration between sponsors and study teams, with integrated central monitoring and issue tracking for streamlined oversight. It delivers actionable insights, fully audit-ready, regulatory compliant, and easily scalable across trial types, phases, and geographies.
Advanced eClinical Tools: IRT and ePRO/eCOA
To further support streamlined operations and data quality, we offer robust IRT and ePRO/eCOA platforms designed to accelerate timelines and enhance patient-centric delivery.
- Purpose-built for complex, global studies, our IRT solution provides end-to-end trial oversight—from site setup to last patient visit—with real-time logistics tracking and integration across systems.
- Our ePRO/eCOA solutions, designed for patient ease-of-use and global compliance, enable reliable, global data capture while supporting decentralized trial workflows.
Let us help you bring clarity, efficiency, and transparency to your complex development program. Check out our Technology solutions.
Agility and knowledge at your fingertips
Resources
6 Data Sources You Should Be Using in Your Site Selection Process
Product Development Checklist: Considerations for Each Stage of the Drug Development Process
resources
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