Clymb Clinical is a Boston-based clinical data services and technology solutions provider helping biotechnology and pharmaceutical organizations run more efficient clinical trials through technology, automation, AI, and open-source innovation.  

We partner with clients across the full clinical trial lifecycle: from protocol design and statistical programming to regulatory submission support offering flexible engagement models that include both expert-led services and licensed technology solutions. 

Our services span biostatistics, statistical programming in SAS and R, SDTM / ADaM / TFL automation, data visualization, data management, medical writing, and CDISC implementation. 

Complementing our services is our proprietary technology suite, the Clymbr Hub: a unified, AI-driven clinical platform that connects the full Protocol-to-CSR workflow. Built on CDISC standards, the platform is available as a licensed solution and includes:  

• SAP Builder for AI-assisted Statistical Analysis Plans authoring 
• TFL Designer for CDISC ARS-compliant TFL Shell design and metadata capture 
• AI Code Generator for SAS and R program generation 
• siera (R-based) and atlas (SAS-based), automated code generation engines  
• TFL Viewer for collaborative TFL review and approval 
• CSR Builder for AI-assisted Clinical Study Report drafting 
• Submify for SDTM and ADaM solutions 

We work as an extension of our clients' teams embedding alongside biostatistics, statistical programming, and clinical functions to support studies from design through submission. Whether through full-service delivery, consultative support, or deployment of our licensed platforms, we adapt to how each team works. 

Our goal is to reduce manual effort, shorten timelines, and enable clinical teams to focus on accelerating the development of new therapies.  

Innovate. Integrate. Improve. 

Clymb Clinical

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Clymb Clinical

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