Medical Writing/Statistical Analysis and Reporting

At ClinicalRM, our statisticians are well versed in industry and academic clinical research methodologies and have vast experience in the statistical design and analysis of clinical and non-clinical studies. They specialize in SAS programming for summary, analysis, and presentation of study data.

We understand the importance of receiving critical data on time. Our expertise allows for collaboration that will result in better, and faster, drug and device decision-making processes for you and your patients.

Our team provides guidance on the statistical issues throughout all stages of your studies and assures that strata, cohorts, and demographics are handled appropriately, along with efficient use of hypothesis tests, modeling, graphing, etc. for analysis of the data. We use the most up to date software including Oracle Clinical™, SAS™, and JMP to manage biomedical data collection and statistical analysis.

We offer the following statistical analysis and reporting services:

• Study Design and Protocol Preparation
• Development of Statistical Sections of the Protocol
• Design of Randomization Schemes
• Preparation of Tables, Listings, & Figures
• Sample Size Determination
• Statistical Analysis Plan
• Statistical Programming
• Support of DSMB/SMC
• Clinical Summary Reports
• Manuscripts
• ISS/ISE
• Consent Forms

 

GENERAL INQUIRY
Corporate Headquarters
800.431.9640
330.278.2343
info@clinicalrm.comFederal Services Operations
301.620.1987
info@clinicalrm.comInternational Operations
800.431.9640
info@clinicalrm.com

 

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