FACULTY FRONTIER™

Decision Intelligence for Clinical Trials

Make better, faster decisions with AI-powered simulation - from trial design and execution to portfolio-level strategy.
Book Demo
Book Demo

Faculty Frontier™ is the Decision Intelligence platform for clinical trial transformation - connecting data & AI investment to optimise speed, cost and quality in the planning and delivery of molecules to market.

See how Frontier is changing enterprise performance through end-to-end decision integration and AI-powered simulation.

Proven impact across Development
Accelerate clinical planning

Reduce trial planning cycles from 10 weeks to ~10 minutes by rapidly generating and comparing design scenarios. Enable earlier stakeholder alignment and faster convergence on the best plan.

Condense trial timelines

Deploy plans directly into workflows. Reduce downstream amendments and costly delays through advanced powered simulation and optimisation, leveraging existing AI investment.

Deliver higher-quality studies

Deliver ~21% more accurate trial plans, whilst tracking and improving performance over time. Increase confidence across teams, and deliver better medicines to patients, faster.

Novartis
AWS
Roche
GSK
FRONTIER FOR CLINICAL TRIALS
Accelerating the Journey from Molecule to Medicine
Solving for a fragmented development pathway

Modern clinical trials are increasingly complex to design and execute. In early development, teams must interpret growing volumes of clinical and operational data to understand how design decisions affect timelines, feasibility and portfolio performance.

Yet functions continue to rely on siloed tools, inconsistent assumptions and manual processes. This fragmentation slows iteration and limits the ability to address risk early. Design cycles stretch into months, recruitment bottlenecks are common, and limited visibility prevents timely intervention.

Empowering teams with AI-powered simulation and optimisation

Faculty Frontier™ is the Decision Intelligence platform built to address this fragmentation - connecting and orchestrating data, AI models, agents and real-world business processes within a decision-focused simulation layer. By providing a shared world view of trials as they process through phases, teams can collaboratively test and optimise critical scientific and operational decisions before they are committed.

In early trial design, Frontier brings together recruitment models, protocol feasibility, site-performance forecasts and competitor benchmarks to evaluate potential trial design scenarios in minutes. Shared workspaces allow teams to explore impact of eligibility criteria, site mix or enrolment strategy on downstream clinical, operational, regulatory and commercial goals.

Embedded explainability and agentic support enable interrogation of underlying assumptions, benchmarking against similar trials, and clear understanding of what is driving delays - from site selection and stock-outs, to screen failure driven by inclusion and exclusion criteria.

Connecting decisions across time, function and hierarchy

Faculty Frontier™ provides a scalable foundation for clinical development leaders, biostatisticians, operational leads and portfolio owners to model additional decisions over time - and understand how changes in one function propagate across the wider system.

Organisations typically begin with early trial design, using Frontier to generate and compare scenarios, surface feasibility and recruitment risk, and align cross-functional teams on an optimal trial plan. As value is demonstrated, platform capabilities extend into adjacent areas such as supply readiness, operational forecasting and launch planning, enabling teams to execute from a shared evidence base.

Frontier is transforming how R&D decisions are made across time (phase I → phase IV), functions (protocol design → commercial planning), and hierarchical levels (portfolio → programme → site). By integrating data and models into a unified simulation layer, leading pharma organisations are now making more coherent decisions end-to-end. The result is a more connected and resilient development organisation - delivering better medicines to patients, faster.

EMPOWERING DECISION-MAKERS ACROSS R&D

Strengthen early scientific decision-making by simulating how trial design parameters influence feasibility, recruitment dynamics and overall study performance. Test alternative assumptions, assess probability of success, and explore the operational implications of different design scenarios within a unified environment. Generate and compare scenarios in minutes, converging quickly on designs that balance scientific objectives with operational reality.

"We spent a year systematically looking at how AI can enable our clinical trials. We can shift the performance of multiple individuals closer to the performance of the best, and I’m convinced that’s where the real value is going to come."

Shreeram Aradhye
President, Development and Chief Medical Officer, Novartis

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Frontier for Clinical Trials

Complete the form to access our latest keynote - exploring how leading life sciences organisations are using Decision Intelligence and AI-powered simulation to deliver better medicines to patients, faster.