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Bristol Myers Squibb accelerates clinical trials by months with Workbench AI platform

“Bristol Myers Squibb accelerates clinical trials by months with Workbench AI platform” documents a Clinical Trials & Research deployment in Pharmaceutical & Life Science at Bristol Myers Squibb. www.accenture.com reports user adoption growth: Under 100 to nearly 900 users in 3 months; this directory has not independently verified that result.

Maintained by Peter Korpak, Founder & Chief AnalystHow evidence is checked

Evidence at a glance

Evidence status:
Automated evidence gate passed
Deployment timeframe:
Not reported by source
Reported outcome metrics:
3 cited below
Directory entry published:
Source link checked:

The source-link check confirms reachability, not independent re-verification of every claim.

Under 100 to nearly 900 users in 3 monthsUser Adoption Growth
Months faster per trialClinical Trial Acceleration
30+Generative AI Solutions Deployed

Source-reported figures — cited source: www.accenture.com

The Challenge

Phase III clinical trials cost between $19 million and over $100 million per trial and involve complex logistics across partners and sites. BMS needed to reduce development timelines and costly inefficiencies to bring breakthrough therapies to patients faster.

The Solution

In partnership with Accenture, BMS implemented over 30 generative AI solutions across R&D, Global Product Development & Supply, and Commercialization. The centerpiece is 'Workbench,' a clinical trial accelerator that fuses AI-driven insights with real-time operational data, delivers role-based recommendations, anticipates issues, and captures institutional knowledge across trial teams.

Results

The approach accelerated BMS clinical trials by months and increased reaction speed to prevent issues. The platform was adopted by over 30 top-priority clinical trial teams and became BMS's official platform for priority trials, standardizing best practices across the organization.

Key Takeaways

  • Generative AI integrated with real-time operational data can compress Phase III clinical trial timelines by months at scale.
  • Role-contextual, personalized platforms drive rapid adoption — users grew 9x in just three months without mandated rollout.
  • AI platforms that capture and forward institutional knowledge help large organizations maintain execution consistency across distributed trial teams.

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Details

Company Size
Enterprise
Evidence status
Automated evidence gate passed
Deployment timeframe
Not reported by source
Directory entry published
Source link checked

Cited source

www.accenture.com

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