A Trusted Partner for Your Statistical Programming Efforts
Experis Solutions provides high-quality, cost-effective statistical programming support to some of the world’s largest life sciences companies through a variety of models including Functional Service Provider (FSP), study-specific or rescue study support, and other resourcing solutions across the clinical trial spectrum. Our clinical development centers in the U.S. and Eastern Europe are home to some of the top clinical talent in the industry.
Our study team leads and engagement managers have decades of industry experience in leading programming teams of all sizes. We offer a variety of services to augment and complement your internal team's efforts.
Analysis Dataset Creation
Experis Solutions programmers are efficient in the creation of value-added datasets, either in a company proprietary standard or an industry standard such as ADaM. Our programmers understand the nuances of clinical data and how to implement complex statistical algorithms. Our lead programmers and statisticians can also draft detailed specifications for use by the programming team.
Tables, Listings, and Graphs Programming
Output displays are the backbone of any regulatory submission. Let our experienced team help create all the in-text and post-text TLGs needed for your clinical study report, annual report or ISS/ISE.
Increasing importance is being placed on the accuracy of the work performed by statistical programmers. Our team is well versed in all approaches to validation/verification, from total independent programming (2nd programmer QC) to a more risk-based approach.
Experis Solutions' highly specialized and experienced PK/PD programmers can be up and running fast. This strong internal network allows them to share knowledge and problem-solve quickly so that your analysts and clinicians are presented with solutions rather than questions. Our programmers are experienced in both NONMEM and NCA data set creation, as well as TLG outputs.
Post-Marketing Clinical Data Analysis
We have a wealth of experience analyzing data from Phase IV clinical trials, as well as publication support. We understand the ad hoc nature of this type of work, and our collaborative, flexible approach is well suited to this environment.
Our experienced team has been working within the different CDISC models for several years, both SDTM and ADaM. Experis Solutions team Leads keep up with all of the changes in the implementation guides produced by CDISC.org, and they develop an understanding of each client’s approach to CDISC compliance. We have mapped legacy data for hundreds of clinical studies to either the SDTM standard or a different proprietary standard.
We understand regulatory filings and where statistical programming fits into the process. We also know that a well-designed electronic portion of a submission can help to facilitate a timely review of the submission by the regulatory agency. Let our experience in this area help get your compound from submission to market more efficiently.
Start-to-finish statistical programming support
Working with Experis Solutions, life sciences clients benefit from:
Over 30 years of statistical programming experience
Established clinical development centers in the U.S. and Eastern Europe
Our refined and proven programming processes that can be customized to meet SOPs
A fast program launch due to our extensive network of qualified clinical professionals
Our proven engagement management process that supports effective communication, quality, and timeliness