Full-Service Clinical Trial Management
CEBIS supports clinical trials from study planning and start-up through project management, site oversight, clinical monitoring, data management, statistical analysis and study closeout. Our teams can provide focused support for individual study functions or coordinate multiple services through one integrated delivery model.
One Coordinated Approach
Across the Clinical Trial
Clinical trials require multiple teams, sites, systems and timelines to work together. CEBIS coordinates study activities around the protocol and project plan so sponsors have clear oversight throughout delivery.
By aligning clinical operations, regulatory, data, safety, quality and supporting functions from the outset, CEBIS helps reduce fragmented handoffs and keeps study teams working toward the same priorities, timelines and deliverables.
Study Planning
Support for translating study requirements into an operational plan, including timelines, responsibilities, countries, sites and supporting functions.
Regulatory & Study Start-Up
Coordination of regulatory and ethics activities, essential documents and site-readiness requirements needed to move the study toward activation.
Site Activation & Enrollment
Site initiation and operational support as participating centers begin recruitment and study activity.
Study Execution & Monitoring
Ongoing project management, site oversight, monitoring, issue follow-up and coordination of study activities.
Data Review & Analysis
Data management, cleaning, reconciliation, statistical analysis and preparation for database lock.
Study Closeout
Coordination of final site activities, documentation, database completion, reporting and study closeout.
Support Across
Clear
Milestone Tracking
Monitor progress against key study activities and timelines.
Risk & Issue Management
Identify operational risks, escalate significant issues and follow actions through resolution.
Cross-Functional Coordination
Align clinical, data, regulatory, safety, supply and quality activities around shared study priorities.
Sponsor Communication
Maintain clear communication around progress, decisions, risks and upcoming milestones.
Clinical Trial Management Across
The operational needs of a clinical study change as a program moves through development. CEBIS can adapt the clinical trial management model around the study phase, design, population and geographic scope.
Phase I & Early Development
Support for early clinical, pharmacokinetic, healthy-volunteer, patient and specialized study requirements.
Phase II–III
Full-service operational execution for multi-site clinical studies, including project management, monitoring, enrollment oversight and data delivery.
Phase IV & Late Phase
Support for post-marketing, observational and other late-phase studies requiring continued operational and data coordination.
Explore Clinical Development - Phase I to IV
Planning a Clinical Development Program?
Tell us about your product, development stage, study design, countries and the support you require. A member of the CEBIS team will discuss the appropriate next steps with you.