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# PK/PD Statistical Programmer - homebased

- **Company:** IQVIA Inc.
- **Location:** Frankfurt am Main, Germany (Remote available)
- **Experience:** Expert
- **Contract:** Permanent contract
- **Skills:** Clean Code Principles, Automation of Tests, Clinical Data Repository, Data Files, Data Structures, R (Programming Language), Data Processing, Data Management
- **Published:** August 19, 2026
- **Apply:** https://iqvia.wd1.myworkdayjobs.com/IQVIA/job/Frankfurt-Hesse-Germany/PK-PD-Statistical-Programmer_R1532189

## About the Role

* We are seeking an experienced PK/PD Statistical Programmer with strong experience in R programming, PK/PD datasets, and NONMEM dataset creation. This role supports Pharmacometrics by producing high-quality, compliant datasets for modeling and analysis, ensuring accuracy from early (unclean) through post-lock clinical data. The ideal candidate brings deep technical expertise, strong problem-solving skills, and a solid understanding of PK/PD principles., + Bachelor's or Master's degree in a health, science, IT, mathematics, or related field.
 + Minimum 6 years of industry experience in clinical data analysis, statistical programming, or pharmacometrics support.
 + Expert-level proficiency in R for data processing, dataset creation, and QC automation.
 + Hands-on experience creating NONMEM datasets, including complex data structures for PK/PD analyses.
 + Strong understanding of SDTM, ADaM, and controlled terminology.
 + Applied knowledge of PK/PD principles and clinical trial concepts.
 + High attention to detail with strong analytical, documentation, and communication skills.
 + Ability to work independently and collaboratively across global, cross-functional teams.

Preferred Skills

 + Experience building or enhancing standardized workflows for NONMEM dataset creation, submission packages, and QC.
 + Experience with R package testing, validation frameworks, or reproducible programming practices.
 + Familiarity with pharmacometrics workflows in clinical or real-world settings.

## Description

+ Program, validate, and deliver NONMEM-ready PK/PD datasets based on SDTM/ADaM standards using advanced R programming skills.
 + Create high-quality PK/PD datasets for both pre-lock and post-lock clinical data.
 + Independently execute programming tasks of medium to high complexity with excellent accuracy and timeliness.
 + Critically review data, identify inconsistencies or gaps, and propose solutions to improve dataset quality and programming efficiency.
 + Perform quality control (QC) of NONMEM datasets, including those produced by external partners.
 + Support preparation of deliverables for regulatory submissions following internal Pharmacometrics guidelines.
 + Conduct QC of customized R packages used for pharmacometrics workflows; enhance or build automated test suites where needed.
 + Liaise with cross-functional teams including Data Management, Biostatistics, Statistical Programming, and Bioanalytical groups to resolve data issues and ensure alignment.
 + Adhere to relevant SOPs, working instructions, and regulatory standards; maintain inspection readiness.
 + Contribute as a technical driver in the development and improvement of new PM standardization initiatives related to dataset creation and QC.


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