PK/PD Statistical Programmer (m/w/d) - homebased

IQVIA; København; On-site; DKK 700,000 - 900,000; Full time

Job summary

IQVIA seeks an experienced PK/PD Statistical Programmer to produce NONMEM‑ready PK/PD datasets using SDTM/ADaM standards. You will shape datasets from unclean to post‑lock data with advanced R skills and collaborate across global teams to ensure accuracy and regulatory readiness.

The role requires 6+ years in pharmacometrics or clinical data analysis, deep PK/PD knowledge, and strong problem‑solving ability.

Qualifications

• 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.

Responsibilities

• 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.

Skills

R programming

PK/PD datasets

NONMEM datasets

SDTM/ADaM understanding

Pharmacometric concepts

Data analysis

Cross-functional collaboration

Education

Bachelor’s or Master’s degree in health, science, IT, mathematics, or related field

Tools

NONMEM

R

Job description

Frankfurt, Hesse, Germany

Paris, France

Barcelona, Spain

Paris, France

Budapest, Hungary

Turku, Finland

Dublin, Ireland

Athens, Greece

Madrid, Spain

Copenhagen, Denmark

Stockholm, Sweden

Full time

R1532189

• 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.

Key Responsibilities

• 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.

Required Qualifications

• 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.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

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