Statistical Programming

Enhancing your statistical computing environment.

Experis provides high-quality, cost-effective Statistical Programming support to some of the world’s largest Life Sciences companies through a variety of models including FSP, project-by-project support, as well as Staff Augmentation resources.

Our clinical facilities in the U.S. and Europe are secure sites that house some of the top clinical talent in the industry. Our dedicated Clinical Practice Recruiters have decades of experience in searching for the right clinical talent, and our management teams screen the candidates thoroughly to make sure they will be the right fit for your project. We offer comprehensive services, including:

  • Analysis Dataset Creation
  • Tables/Listings/Graphs Programming
  • Validation/QC/Verification Programming
  • PK/PD Support
  • Post-Marketing Clinical Data Analysis
  • CDISC/Data Mapping
  • eSubmission Support

You’ll benefit from:

  • 30 years of clinical development experience
  • Established clinical support facilities in the U.S. and Europe
  • Refined and established FSP processes to bring the most value
  • Fast program launch due to our extensive network of qualified clinical professionals
  • Proven Engagement Management process to ensure quality and timeliness
  • Understanding of industry regulations and requirements

Start-to-finish statistical programming support

Analysis Dataset Creation

Experis 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/or Statisticians can also draft detailed specifications for use by the programming team.

Tables/Listings/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.

Validation/QC/Verification Programming

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.

PK/PD Support

Experis has highly-specialized and experienced professionals in place who can be up and running much quicker than a nonexperienced PK/PD programmer. 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

Our team has 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.

CDISC/Data Mapping

Our experienced team has been working within the different CDISC models for several years, both SDTM and ADaM. Our 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. In addition, we have mapped legacy data for hundreds of clinical studies to either the SDTM standard or a different proprietary standard.

eSubmission Support

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.

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