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# Pharmacometrics Support Programmer

- **Company:** ICon GmbH & Co. KG
- **Location:** Frankfurt am Main, Germany
- **Experience:** Expert
- **Contract:** Permanent contract
- **Skills:** Clinical Data Repository, Computer Programming, R (Programming Language), Information Technology, Data Management
- **Published:** October 6, 2026
- **Apply:** https://www.jobfinder.de/job/pharmacometrics-support-programmer/

## About the Role

efficiency.Actively contribute to the development and implementation of new pharmacometric standardisation initiatives.Ensure all deliverables comply with applicable SOPs, working instructions, regulatory requirements, and ICH-GCP guidelines.Maintain inspection readiness through ongoing training and adherence to quality standards.What We're Looking ForBachelor's degree in a Life Science, Health Science, Statistics, Computer Science, IT, or related discipline.Minimum of 6 years' experience within the pharmaceutical, biotechnology, or CRO industry.Strong programming expertise in R.Experience developing and quality controlling NONMEM PK/PD datasets.Working knowledge of PK/PD principles and pharmacometric workflows.Strong understanding of SDTM, ADaM, and CDISC standards, including controlled terminology.Experience supporting NONMEM file creation, quality control, submissions, and standardisation activities.Strong attention to detail and commitment to data quality.Excellent written and verbal
communication skills in English.Desired SkillsExperience reviewing and managing outsourced programming deliverables.Experience validating or quality controlling customised R packages.Demonstrated ability to identify process improvements and drive standardisation initiatives.Ability to work effectively across global, cross-functional teams.Why Join Us?Opportunity to work within a globally recognised Clinical Pharmacology & Pharmacometrics function.Contribute directly to innovative drug development programmes.Work in a highly collaborative and scientifically driven environment.Be part of ongoing innovation and standardisation initiatives within pharmacometrics and clinical data science.Use your expertise to influence best practices and improve the efficiency and quality of pharmacometric deliverables.If you are passionate about leveraging R programming, pharmacometrics, and data quality excellence to support drug development, we'd love to hear from you.#LI-JF1Employment with ICON

## Description

key role in ensuring high-quality pharmacometric data is delivered on time and to the highest regulatory standards.Key ResponsibilitiesDevelop and quality control NONMEM PK/PD datasets using SDTM and ADaM data sources.Support pharmacometric modelling activities by delivering accurate, complete, and submission-ready datasets.Perform quality review of internally and externally produced NONMEM datasets.Collaborate with Data Management, Statistical Programming, Statistics, Clinical Pharmacology, and Bioanalytical teams to resolve data issues and ensure project timelines are met.Contribute to the preparation of regulatory submission projects in accordance with internal pharmacometrics guidelines.Conduct quality control testing of customised R packages used to standardise pharmacometric workflows.Develop and maintain testing frameworks and validation processes for departmental R tools and packages.Identify data discrepancies, process improvements, and opportunities for greater automation and