IQVIA
Senior Statistical Programmer - FSP(m/w/x)
Full-timeWith HomeofficeSenior
Frankfurt am Main
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IQIQVIA
PK/PD Statistical Programmer(m/w/x)
Frankfurt am Main
Full-timeWith Home OfficeSenior
Nejo AI Summary
Programming and validating NONMEM-ready datasets for clinical trial data in drug development. 6+ years industry experience in clinical data analysis and expert R proficiency required. Work in a global clinical research environment.
Requirements
- Bachelor's or Master's degree in health, science, IT, mathematics, or related field
- Minimum 6 years industry experience in clinical data analysis, statistical programming, or pharmacometrics support
- Expert-level proficiency in R
- Hands-on experience creating NONMEM datasets
- Strong understanding of SDTM, ADaM, and controlled terminology
- Applied knowledge of PK/PD principles and clinical trial concepts
- High attention to detail, strong analytical, documentation, and communication skills
- Ability to work independently and collaboratively
- Experience building/enhancing NONMEM dataset workflows
- Experience with R package testing, validation frameworks, or reproducible programming
- Familiarity with pharmacometrics workflows
Tasks
- Program, validate, and deliver NONMEM-ready PK/PD datasets.
- Create high-quality PK/PD datasets for pre-lock and post-lock clinical data.
- Execute complex programming tasks independently.
- Critically review data.
- Identify data inconsistencies and gaps.
- Propose solutions for dataset quality and programming efficiency.
- Perform quality control on internal and external NONMEM datasets.
- Assist in preparing deliverables for regulatory submissions.
- Perform QC on customized R packages.
- Enhance or build automated test suites.
- Collaborate with cross-functional teams to resolve data issues.
- Ensure alignment with cross-functional teams.
- Adhere to SOPs, working instructions, and regulatory standards.
- Maintain inspection readiness.
- Drive PM standardization for dataset creation and QC.
Work Experience
- 6 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- R
- NONMEM
- SDTM
- ADaM
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of IQVIA and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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IQIQVIA
PK/PD Statistical Programmer(m/w/x)
Frankfurt am Main
Full-timeWith Home OfficeSenior
Nejo AI Summary
Programming and validating NONMEM-ready datasets for clinical trial data in drug development. 6+ years industry experience in clinical data analysis and expert R proficiency required. Work in a global clinical research environment.
Requirements
- Bachelor's or Master's degree in health, science, IT, mathematics, or related field
- Minimum 6 years industry experience in clinical data analysis, statistical programming, or pharmacometrics support
- Expert-level proficiency in R
- Hands-on experience creating NONMEM datasets
- Strong understanding of SDTM, ADaM, and controlled terminology
- Applied knowledge of PK/PD principles and clinical trial concepts
- High attention to detail, strong analytical, documentation, and communication skills
- Ability to work independently and collaboratively
- Experience building/enhancing NONMEM dataset workflows
- Experience with R package testing, validation frameworks, or reproducible programming
- Familiarity with pharmacometrics workflows
Tasks
- Program, validate, and deliver NONMEM-ready PK/PD datasets.
- Create high-quality PK/PD datasets for pre-lock and post-lock clinical data.
- Execute complex programming tasks independently.
- Critically review data.
- Identify data inconsistencies and gaps.
- Propose solutions for dataset quality and programming efficiency.
- Perform quality control on internal and external NONMEM datasets.
- Assist in preparing deliverables for regulatory submissions.
- Perform QC on customized R packages.
- Enhance or build automated test suites.
- Collaborate with cross-functional teams to resolve data issues.
- Ensure alignment with cross-functional teams.
- Adhere to SOPs, working instructions, and regulatory standards.
- Maintain inspection readiness.
- Drive PM standardization for dataset creation and QC.
Work Experience
- 6 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- R
- NONMEM
- SDTM
- ADaM
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of IQVIA and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
IQVIA
Industry
Pharmaceuticals
Description
IQVIA is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients.
Not a perfect match?
- IQVIA
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