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Specialized Site Network for Early-phase Oncology Success

September 03, 2025

Early-phase oncology trials are complex, demanding precision, rapid execution, and specialized expertise. Yet, too often, the operational burden falls on clinical sites―already overworked and stretched thin. Within large, volume-driven CRO networks, this creates a system that prioritizes scale over quality, offering minimal site support, delaying timelines, and ultimately compromizing trial outcomes.   

Purpose-built site network designed for biotech

Catalyst Oncology takes a different approach―offering a purpose-built, multiregional site network designed specifically for early-phase oncology trials. Built on rigorously selected sites with proven oncology expertise, this network thrives on trust-based partnerships that streamline operations and eliminate inefficiencies. By easing the burden on sites, we foster a highly motivated network that consistently meets enrollment targets―accelerating timelines, enhancing data integrity, and delivering meaningful clinical results.

Global, relationship-driven site solutions that deliver

Access to global footprint
  • ~20 specialized sites located across the US, Spain, UK and Australia
  • 50+ active trials at network sites
Collaborative, relationship-driven approach
  • Dedicated relationship managers
  • First right of refusal for novel protocols with slot and activation commitments
  • Early access to next-gen oncology therapies
  • Ongoing, consistent support
Operational efficiency and streamlined start-up
  • Master templates, core feasibility, waived SEVs and site checklists
  • Real-time performance feedback and reliable forecasts
  • Expedited launch, elimination of inefficiencies, reduced site fatigue
Tailored, data-driven solutions
  • Assessments of site capabilities and financial needs
  • Customized tech and resourcing strategies

Exclusively biotech-focused

Built to work exclusively with biotechs, our flexible processes and approach allow us to listen first, align goals, and execute with an eye toward rapid shifts when a protocol is amended or Breakthrough designation moves a product straight from Phase I to registration.

Seasoned oncology experts

With an average of 9+ years of oncology experience for key roles (PM, CTL, DM, Bios, Clinical Science), our oncology specialty guarantees you a seasoned team across all functions.

A transparent people-first culture with industry leading retention

We are responsive and attentive to the needs of both our customers and staff. Our industry-leading employee and project team retention guarantees program continuity, increased efficiency, and happy investigative sites.

Active next-gen oncology experience


Working both locally and globally across Phases I through III in a range of solid tumor and hematologic indications, we understand the nuances of complex study designs, novel endpoints, and cutting-edge technologies. 

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