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# Statistical Programmer I FSP

- **Company:** Cytel Inc.
- **Location:** Oklahoma City, OK, United States
- **Experience:** Experienced
- **Contract:** Permanent contract
- **Skills:** Computer Programming, SAS (Software), Data Processing, Information Technology
- **Published:** September 19, 2026
- **Apply:** https://dejobs.org/x/x/7AE0EBE1F69943E39A41041177EC8C1A/job/

## About the Role

* A minimum of 4 years of Undergraduate study and 2 additional years of Graduate-level education
 * Academic training in both of the following 2 categories (or closely related fields)
 * Statistics, Epidemiology, or Data Science
 * Computer Science, Mathematics, or Computational Science
 * Foundational data manipulation, analysis and reporting skills
 * Familiarity with drug development life cycle and a passion to learn and expand knowledge
 * Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
 * Excellent oral and written English communication skills
 * Ability to provide quality output and deliverables, in adherence with challenging timelines
 * Willingness and ability to learn and follow Company's standard processes and procedures.
 * Ability to effectively learn and perform statistical programming and related tasks

## Description

Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program., We are looking for a Recent Graduate to perform and act as a Statistical Programmer, where you will leverage your education to develop and expand programming skills, supporting one or more Phase I-IV clinical trials. This is a great opportunity to start a career in Clinical Life Sciences, supported by Cytel and embedded in a trusted partner.

As a Statistical Programmer, your responsibilities will include:

 * Performing data manipulation, analysis, and reporting of clinical trial data, both safety and efficacy, utilizing SAS programming
 * Applying your SAS programming skills, to create and validate datasets/analysis files, tables, listings, and figures ( TLF s)
 * Generating ad-hoc reports
 * Preparing and validating submission packages
 * Applying your understanding/experience with Efficacy analysis
 * Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.
 * Being adaptable and flexible when priorities change