Bhavin Busa
Principal & Co-founder
Clinical data services company
Cost-effective clinical trial solutions for biotech and pharmaceutical companies
Clymb Clinical combines biometrics expertise, open-source technology, and the Clymbr Hub platform to deliver flexible, cost-effective clinical trial solutions to biotech and pharmaceutical companies worldwide.
How we run clinical data01 / 05
inputs
Source data, labs, and external vendor feeds land in the governed environment.
What clinical trial solutions does Clymb Clinical provide?
Clymb Clinical provides flexible, cost-effective clinical trial solutions for biotech and pharmaceutical companies. We combine biostatistics, statistical programming, clinical data management, and submission-ready reporting with the Clymbr Hub automation platform. Deliverables are produced inside a validated statistical computing environment by global teams in the US, Armenia, South Africa, and India.
- Sponsors
- Emerging biotech, mid-size pharma, and large pharmaceutical companies
- Delivery models
- Outsourcing, FSP, consulting, and Clymbr Hub platform licensing
- Standards
- CDISC SDTM, ADaM, ARS/ARD, Define.xml, and 21 CFR Part 11 alignment
Clymb at a glance
A data & technology-centric biometrics partner.
Founded in 2022 by Bhavin Busa and Colin Izzo with the vision of optimizing technology in the biometrics niche. Headquartered in Burlington, MA.
4
Sites Across the Globe
Headquartered in the US with sites in Armenia, South Africa and India.
40+
Customers
Utilizing the Clymbr Hub or Clymb's Services and Outsourcing Team.
3,000+
Platform Users
Across our Enterprise and Community versions of Clymbr Hub.
10+
Years
Average team member experience.
15+
Submissions
Across various therapeutic areas since Clymb's Inception.
2022
Founded
Burlington, MA — built to optimize technology in the biometrics niche.
CDISC partnership
We partner with CDISC on the Analysis Results Standard (ARS), the eTFL Portal, and CDISC 360i (AC/DC standards) — so the standards we build to are the standards we help write.
Why Clymb?
At Clymb Clinical, we're driven by a constant desire to innovate, integrate, and improve. Those three principles are what let us build tools and services that actually make a difference in clinical research and development — and help our clients reach their goals more efficiently.
Revolutionizing clinical data analytics
Our aim is to transform clinical data analytics and lead the data services industry — innovating relentlessly to accelerate clinical trials.
Innovate. Integrate. Improve.
Our core values
Data-centric by design. Clinical data outsourcing and consulting services built on the latest technology and advanced data analytics.
Pioneering
We're not interested in maintaining the status quo. At Clymb we encourage everyone to challenge conventions and keep pushing boundaries.
Unified
Diverse elements, thoughts, ideas, and individuals — but collectively one unified team focused on efficient service at the highest quality.
Trust
Trust is the foundation of our relationships with clients, partners, and colleagues. We're transparent, reliable, and we deliver on what we promise.
Virtuous
We hold ourselves to unwavering integrity in every action. Our commitment to honesty and ethical conduct is non-negotiable.
Meet our leaders
Colin Izzo
Principal & Co-founder
Navin Dedhia
VP of Engineering and AI Solutions
While we're headquartered in Burlington, MA, our team works virtually from locations around the world — enabling a flexible, dynamic working environment.
Cost-effective clinical trial solutions: frequently asked questions
What clinical trial solutions does Clymb Clinical provide?
Clymb Clinical provides flexible, cost-effective clinical trial solutions for biotech and pharmaceutical companies, including biostatistics, statistical programming, clinical data management, SDTM/ADaM mapping, SAP authoring, TFL generation, CSR support, and full-service outsourcing through a global delivery model.
Why are Clymb Clinical's solutions cost-effective for biotech and pharma?
We combine open-source technology, reusable CDISC-aligned standards, and the Clymbr Hub automation platform with experienced global teams. This reduces manual effort, accelerates deliverables, and lowers total study cost without sacrificing quality or compliance.
Does Clymb Clinical work with small and mid-size biotech companies?
Yes. Our service models are designed to scale with emerging biotech, mid-size pharma, and large pharmaceutical companies. We offer functional service provider (FSP), full outsourcing, and consulting engagements tailored to each sponsor's size, maturity, and trial complexity.
What services are included in Clymb Clinical's outsourcing model?
Our outsourcing and FSP teams cover biometrics, statistical programming, data management, medical writing support, quality control, submission readiness, and ongoing study maintenance. Deliverables are produced inside a validated statistical computing environment with full audit trails.
How does Clymb Clinical ensure data quality and regulatory compliance?
We follow CDISC SDTM, ADaM, ARS/ARD, and Define.xml standards, operate in a 21 CFR Part 11 aligned environment, and build quality checks into every workflow. Our CDISC partnership means the standards we implement are the standards we help shape.
What is Clymbr Hub and how does it reduce trial costs?
Clymbr Hub is Clymb Clinical's unified AI-powered platform for Protocol-to-CSR automation. It connects Data Mapper, SAP Builder, TFL Designer, Code Generators, TFL Viewer, and CSR Builder in one statistical computing environment, cutting manual effort and rework across the reporting lifecycle.
Where are Clymb Clinical's teams located?
Headquartered in Burlington, MA, Clymb Clinical operates global sites in Armenia, South Africa, and India, enabling around-the-clock support, flexible resourcing, and cost-efficient delivery for sponsors worldwide.
How can I request a quote or demo for my clinical trial?
Contact us through the Request a Demo & Pricing form or email info@clymbclinical.com. Our team will review your protocol, scope, and timelines, then recommend a cost-effective service or platform package aligned to your study needs.
Join our team
Passionate about data and problem-solving? We're looking for data analysts, engineers, scientists, and developers to help us turn data into insight and action.
Let's Connect
Tell us what you need , we'll reply within one business day.
We partner with pharma, biotech, CROs, and technology vendors on platform access, outsourcing, and FSP delivery.
Pharma / BiotechCROVendor / Partner