Clinical trial operations

Simplify and scale clinical trial operations
Streamline clinical trial operations with Oracle’s unified applications for portfolio planning, study startup, electronic trial master file management, and clinical trial management. Deliver scalable, secure, and compliant automation through Oracle Cloud Infrastructure (OCI). Integrate systems seamlessly and generate actionable analytics—simplifying oversight and supporting clinical trial success.

Clinical trial operations solutions

Accelerate clinical trial success with automated, AI-powered solutions that help simplify operations, enhance data quality, and support compliance.

Plan portfolios with confidence

Enable sponsors and contract research organizations (CROs) to quickly create accurate study budgets, timelines, and resource plans. Streamline scenario modeling and vendor comparisons to support fast, data-driven decisions by using activity-based costing, benchmarking, and advanced analytics.

Portfolio planning for sponsors

Oracle Life Sciences ClearTrial for sponsors helps streamline clinical trial planning, budgeting, and management with cloud-based automation. Centralize study data, connect workflows across enterprise systems, and leverage built-in interoperability for consistent processes. Gain real-time operational insights, coordinate resources, and align activities with organizational goals—supporting transparency, collaboration, and regulatory compliance throughout the clinical development lifecycle.

Portfolio planning for CROs

Oracle Life Sciences ClearTrial for CROs helps optimize proposal development, resource planning, and project delivery with advanced automation and smart budgeting tools. By seamlessly connecting core study data with project management and financial systems, ClearTrial helps streamline operational workflows and enable transparent, scalable collaboration. Integrated interoperability supports near real-time data sharing and coordination with sponsors, helping alleviate manual effort, enhance accuracy, and enable timely, competitive CRO services to address customer demands and operational challenges.

Drive study startup success

Streamline site feasibility, selection, activation, and patient recruitment for your study startup with Oracle Life Sciences solutions. Accelerate site evaluation by leveraging data-driven insights; optimize enrollment through precise patient matching; and support efficient, compliant trial launches—helping strengthen study outcomes.

Site selection

Oracle Life Sciences Site Select enables users to identify, evaluate, and prioritize clinical trial sites by leveraging advanced automation and data-driven analytics. Our solution streamlines site selection workflows by integrating near real-time performance metrics, investigator databases, and feasibility data into a single, unified platform. With interoperability features that connect to external data sources and existing clinical trial management systems, our solution supports efficient collaboration and consistent decision-making. This approach helps organizations address site selection complexity, support regulatory readiness, and enhance trial performance and predictability.

Site feasibility

Oracle Life Sciences Site Feasibility empowers sponsors to evaluate, compare, and select clinical trial sites using automated assessments and data-driven analytics. Centralize site survey data, investigator profiles, and performance metrics in a single platform to streamline feasibility workflows. Integration with trial management and site selection systems enables coordinated decision-making and secure data sharing—helping study teams manage site identification complexity, promote consistent evaluations, and make informed site selections.

Site activation

Oracle Life Sciences Site Activate empowers teams to accelerate the clinical trial startup process by centralizing document workflows, regulatory packet management, and communications on a unified cloud-based platform. Automate and track critical milestones, enable collaboration among sponsors, sites, and CROs, and maintain audit-ready transparency. Oracle Life Sciences Site Activate supports efficient submission, review, and approval cycles, helping facilitate regulatory compliance, minimize delays, and accelerate launch with quality.

Patient recruitment

Oracle Life Sciences Patient Recruitment empowers health systems to coordinate, track, and manage clinical trial recruitment across multiple sites with automated workflows and centralized dashboards. Leverage data-driven targeting and integrated outreach tools to streamline candidate identification and engagement. Interoperability with site management systems and EHRs facilitates cohesive communications and efficient referral management—helping organizations overcome recruitment challenges, enhance oversight, and align enrollment efforts with study objectives.

Simplify compliance

Centralize and automate clinical trial documentation on a secure cloud platform to help enhance collaboration, support compliance, and simplify audit readiness with integration capabilities and streamlined workflows.

Electronic trial master files

Oracle Life Sciences eTMF Cloud Service streamlines the organization, management, and access of essential trial documentation on a secure, cloud-based platform. Automate document workflows and centralize regulatory content to help enhance collaboration and support audit readiness across teams and stakeholders. Integration capabilities with clinical trial management and site systems help enable efficient data exchange and consistent document tracking—supporting compliance efforts, helping facilitate inspections, and enabling timely decisions throughout the clinical trial lifecycle.

Gain centralized oversight and streamline operations

Transform how you manage clinical trials with a comprehensive, configurable solution designed to optimize every phase of the trial lifecycle. Centralize key trial processes including study planning, site and investigator management, operational tracking, document management, payments, and risk assessment. Support compliance, oversight, and overall trial efficiency with an integrated approach to clinical trial management.

Clinical trial management system

Oracle Life Sciences CTMS empowers users to manage and monitor clinical trial operations with centralized tracking of study activities, site performance, and regulatory documentation. Advanced automation and configurable workflows unify data management and streamline processes, enabling timely collaboration among sponsors, CROs, and sites. Interoperability with key systems—such as electronic data capture (EDC) and electronic trial master file (eTMF)—supports data integrity and comprehensive oversight, helping organizations address operational complexity, enhance compliance, and facilitate consistent trial execution across their research portfolio.