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Flatiron Trials

Traditional approaches to oncology trials are unsustainable and no longer meet the industry’s needs. It’s time to evolve. Flatiron leverages real-world data and AI, pragmatic design principles, tech-enabled research sites, and fit-for-purpose CRO services to reimagine study design and execution for your oncology trials and prospective studies.

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Flatiron helps oncology sponsors run faster, smarter trials

Flatiron is rebuilding trial delivery for modern oncology—with real-world data (RWD), AI and site-based technology.

We offer full-service support for the design and execution of late-phase interventional, observational, and pragmatic trials, including protocol design, start-up, execution, and close-out. 

Our approach delivers fit-for-purpose evidence with greater reliability, improved efficiency, and reduced burden for sites and patients.

Choose a proven partner to execute your evidence strategy

25%+ more eligible patients

via site insights and more pragmatic inclusion and exclusion (I/E) criteria informed by oncology RWD from over 5M patients

95% better screening efficiency

via real-time multimodal data, AI-assisted centralized review, and timely eligibility alerts at the point of care

10x faster data entry, 90% fewer queries

via EHR-to-EDC technology and AI-driven protocol adherence

1,300+ trials active in 2 years

within the Flatiron Research Network, a tech-enabled site network comprised of 110+ U.S. community sites, health systems, and academic medical centers

hear from our customers

“It was really easy… fewer people were required to run this study. I would like to see more [pragmatic] studies like this.”

Sue Moore

Director of Clinical Research at Virginia Cancer Institute

“Enrollment was 6.5x faster and 20–30% cheaper compared to a traditional trial.”

Top-5 pharma leader on an ongoing post-marketing oncology study

Deploy Flatiron Trials to power Phase IIIB-IV oncology trials

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Smarter protocols

Enhance study design and site selection with insights drawn from multi-modal RWD. Optimize protocols for feasibility, refine I/E criteria to improve patient eligibility, and identify sites with a high concentration of trial-eligible patients with Protocol Optimization by Flatiron. 

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Faster recruitment

Accelerate enrollment with tech-enabled patient pre-screening integrated at our network of research-ready sites. Surface matches at the exact point of eligibility and ensure faster enrollment with reduced site burden with Patient Identification by Flatiron.  

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Cleaner data

Streamline data acquisition by enabling seamless transfer of study data from the EHR to the EDC system. Ensure faster and more accurate data collection and reduce site workload by minimizing manual data entry with Flatiron Clinical Pipe™.

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Streamlined study start-up

Simplify study startup with central management of protocol, ICF, and IRB coordination, site feasibility, contracting and budgets, vendor setup and oversight, and regulatory submissions.

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Efficient operations

Ensure smarter, faster trial operations with a dedicated team of 150+ clinical trial experts. We provide centralized operations, project management, site onboarding and support, software deployment and training, and a combination of on-site, remote and risk-based monitoring. 

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Data and safety

Safeguard patient safety and ensure data integrity with centralized oversight and monitoring. Flatiron’s clinical data managers lead data management and reporting, safety management, clinical study report coordination, database lock, and study closeout and archival.

USE CASES

Accelerate evidence generation across key use cases

Explore more from Flatiron

Explore our entire clinical research product suite

Our clinical research product portfolio reduces burden through technology-supported trials and operational efficiencies, lowers costs and accelerates drug delivery to a diverse patient population, and supports teams from trial design up to FDA submission.

PRODUCTS AND SERVICES INCLUDE:

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Tell us more about your clinical research needs.