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# Data Standards Engineer

- **Company:** IQVIA LLC
- **Location:** Reading, UK
- **Experience:** Expert
- **Salary:** £49,000.0 - £89,000.0
- **Contract:** Permanent contract
- **Skills:** Java (Programming Language), C Sharp (Programming Language), Clinical Data Management, Data Governance, R (Programming Language), Python (Programming Language), Metadata Repositories, Productivity Software, SAS (Software), Julia, Information Technology, Health Level Seven International
- **Published:** August 27, 2026
- **Apply:** https://www.adzuna.co.uk/jobs/details/5856707684

## About the Role

* Bachelors degree in computer science, statistics, or a related area
 * Experience with CDISC Standards, specifically SDTM and ADaM
 * Experience on industry teams involved in standards such as CDISC, HL7, or Transcelerate
 * Strong communication skills
 * 10 years SAS programming experience or other related programming language experience preferred
 * Knowledge of macro or subroutine development is expected
 * Knowledge and experience in two or more programming languages such as SAS, R, Python, Julia, C#, Java, or other language
 * Relevant statistical programming experience with pharmaceutical clinical trial data preferred
 * Experience in mentoring and developing others in the use of CDISC standards
 * Experience in submissions to regulatory authority preferred

## Description

* Support us and our clients as an authority in the use of CDISC Standards through communication, collaboration, training, and mentorship
 * Partner with project statisticians and programming teams to develop global tools to support project programming needs in the use of CDISC Standards
 * Lead the implementation of productivity tools for us and our clients that improve compliance, efficiencies, and timeliness of deliverables
 * Provide training and mentorship in the use of technology and systems, such as metadata repositories, to support our and our clients use
 * Assure that work delivered to clients meets minimum submission requirements as defined by FDA Guidance Documents and other regulatory guidance
 * Guide clients in the use of CDISC standards through governance teams
 * Monitor regulatory authority and standards organization sites for updates and inform leadership of updates
 * Work on other initiatives as a CDISC representative
 * Interact with various CDISC-sanctioned teams in the development of standards
 * Represent us in the industry as a leader in the use of standards and automation
 * Support leadership in the development of processes and tools which enable CDISC compliance

Technologies:

 * C#
 * HL7
 * Support
 * Java
 * Julia
 * Python
 * SAS


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