CE3 Inc.
Catalyst Clinical Research is a flexible, innovative clinical development organization that provides highly customizable solutions to the global biopharmaceutical industry. With a focus on oncology through Catalyst Oncology and multi-therapeutic services via Catalyst Flex, the company leverages over a decade of customer-centric solutions, expert teams, and innovative technologies to drive breakthrough clinical studies. Catalyst is committed to supporting its global team and clients with a culture of listening, flexibility, collaboration, commitment, and learning. The company aims to inspire people to design and deliver better clinical trials, emphasizing responsiveness, collaboration, and tailored solutions to meet the complex needs of the industry.
Industries
Nr. of Employees
small (1-50)
CE3 Inc.
Products
Clinical database and EDC solutions
Clinical database builds and electronic data capture solutions for clinical trials, including large database design and data cleaning processes.
AI-enabled evidence generation and report automation
Platform capabilities applying AI/ML and NLP to automate evidence synthesis and study report generation for clinical development and post‑launch activities.
CTMS study build and configuration services
Study build, configuration, and validation services for CTMS/EDC platforms to ensure operational readiness and standardized study workflows.
Pharmacovigilance system implementation services
Implementation and integration of cloud-based safety and case management systems, plus operational support to enable real-time access to adverse event data and streamlined case workflows.
Clinical database and EDC solutions
Clinical database builds and electronic data capture solutions for clinical trials, including large database design and data cleaning processes.
AI-enabled evidence generation and report automation
Platform capabilities applying AI/ML and NLP to automate evidence synthesis and study report generation for clinical development and post‑launch activities.
CTMS study build and configuration services
Study build, configuration, and validation services for CTMS/EDC platforms to ensure operational readiness and standardized study workflows.
Pharmacovigilance system implementation services
Implementation and integration of cloud-based safety and case management systems, plus operational support to enable real-time access to adverse event data and streamlined case workflows.
Services
Comprehensive clinical development services for oncology programs including protocol design, site management, monitoring, data management, biometrics, and regulatory support.
Modular resourcing and managed services (project management, monitoring, clinical operations staff) to augment sponsor or CRO teams on a flexible, project basis.
Database build, eCRF design, data cleaning workflows, and multi‑platform EDC support for clinical trials.
Statistical analysis plans, statistical programming, endpoint analyses, and biometrics support to generate regulatory-standard outputs and trial-ready deliverables.
Preparation of regulatory and scientific documents and use of automation technologies to streamline document generation and evidence synthesis.
Continuous safety surveillance, medical monitoring, and pharmacovigilance operations for clinical trials, supported by cloud-based safety system implementation and case management.
Comprehensive clinical development services for oncology programs including protocol design, site management, monitoring, data management, biometrics, and regulatory support.
Modular resourcing and managed services (project management, monitoring, clinical operations staff) to augment sponsor or CRO teams on a flexible, project basis.
Database build, eCRF design, data cleaning workflows, and multi‑platform EDC support for clinical trials.
Statistical analysis plans, statistical programming, endpoint analyses, and biometrics support to generate regulatory-standard outputs and trial-ready deliverables.
Preparation of regulatory and scientific documents and use of automation technologies to streamline document generation and evidence synthesis.
Continuous safety surveillance, medical monitoring, and pharmacovigilance operations for clinical trials, supported by cloud-based safety system implementation and case management.
Expertise Areas
- Oncology clinical development
- Clinical trial management
- Early-phase and late-phase trial design and execution
- Clinical data management and EDC
Key Technologies
- Electronic data capture (EDC) and clinical database systems
- Clinical trial management systems (CTMS)
- EHR to EDC data integration
- Cloud-based safety and case management systems
News & Updates
Catalyst demonstrates unwavering commitment to clients, adapting and flexing with needs. Wilmington, N.C., May 19.
Catalyst welcomes new Vice President Sarah St. John, PhD, to the business development team.
Catalyst again named one of the fastest-growing private companies, making the list for the fifth year.
Exploring innovation, patient-centricity, and operational excellence in trials.
Transforming drug development with AI.
Strategies for success in evolving clinical trial landscape.
Catalyst demonstrates unwavering commitment to clients, adapting and flexing with needs. Wilmington, N.C., May 19.
Catalyst welcomes new Vice President Sarah St. John, PhD, to the business development team.
Catalyst again named one of the fastest-growing private companies, making the list for the fifth year.
Exploring innovation, patient-centricity, and operational excellence in trials.
Transforming drug development with AI.
Strategies for success in evolving clinical trial landscape.