Clinical Trial Analysis and Consulting

For over 10 years, StatWorks has provided expert advice and services to a variety of biopharma customers in the design, collection, analysis, and reporting of their clinical trials. We support large and small customers in all phases of development. Get the experience of a big company and the service and value of a small company.

Biostatistics

We pride ourselves on our analytical capabilities and our ability to think critically about your trial and its results. We add significant value to our customers with expertise by focusing on the end product, statistics about your primary objective, in the early stages of a trial and its design. We take great care to design in quality and we obsess about every detail throughout the analysis.

Data Management

We provide full service data management including CRF design, paper and EDC studies, data validation, query management, data integration, and medical coding. We've worked with a variety of data providers to integrate ECG, lab, PK, and other data sources. We use CDISC® standards and can produce to SDTM FDA-compliant datasets.

 

Medical Writing

StatWorks has helped produced numerous study reports and other study documents in its 11 year history. We've participated in several NDA and other international submissions. In addition, we've supported manuscript production as well.

Technology Services

StatWorks provides project web site services, electronic data capture (EDC), programming services, and other trial-related technology and integration services.