PK/PD Statistical Programmer (m/w/d) - homebased
IQVIA Madrid
Experteer Overview
In this role you will develop and QC NONMEM-ready PK/PD datasets from SDTM/ADaM sources, enabling robust pharmacometrics analyses. You will work with cross-functional teams to ensure data quality from unclean to post-lock stages and support regulatory deliverables.You’ll drive automation and standardization of PK/PD data workflows, improving efficiency and compliance. This position offers the chance to shape data pipelines used in modeling and submissions within a global, technically skilled environment.
Compensaciones / Beneficios- Program, validate, and deliver NONMEM-ready PK/PD datasets using advanced R and SDTM/ADaM standards
- Create high-quality PK/PD datasets for pre- and post-lock clinical data
- Execute moderately to highly complex programming tasks with accuracy and timeliness
- Review data for inconsistencies, propose data quality improvements
- QC NONMEM datasets, including work produced by external partners
- Support regulatory submission deliverables following internal guidelines
- QC and possibly extend R packages used in pharmacometrics workflows, build/test automation
- Collaborate with Data Management, Biostatistics, Statistical Programming, and Bioanalytical groups
- Bachelor's or Master's degree in health, science, IT, mathematics, or related field
- 6+ years in clinical data analysis, statistical programming, or pharmacometrics support
- Expert-level R for data processing, dataset creation, and QC automation
- Hands-on experience creating complex NONMEM datasets for PK/PD analyses
- Strong understanding of SDTM, ADaM, and controlled terminology
- Applied PK/PD knowledge and clinical trial concepts
- Attention to detail with good analytical, documentation, and communication skills
- Ability to work independently and with cross-functional teams
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