Senior PK/PD Statistical Programmer (R & NONMEM)

IQVIA LLC

Reading

Hybrid

GBP 65,000 - 90,000

Full time

2 days ago
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Job summary

IQVIA LLC in Reading, United Kingdom, seeks an experienced PK/PD Statistical Programmer to join our pharmacometrics team. You will program, validate, and deliver NONMEM-ready PK/PD datasets based on SDTM/ADaM standards using advanced R skills, ensuring accuracy from unclean to post‑lock clinical data.

The role requires 6+ years in clinical data analysis or pharmacometrics, expert R proficiency, and hands-on NONMEM dataset creation.

Qualifications

  • Bachelor’s or Master’s degree in health, science, IT, mathematics, or related field.
  • 6+ years of industry experience in clinical data analysis or pharmacometrics support.
  • Expert-level proficiency in R for data processing, dataset creation, and QC automation.
  • Hands-on experience creating NONMEM datasets, including complex PK/PD structures.
  • Strong understanding of SDTM, ADaM, and regulatory submissions.

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- and post-lock clinical data.
  • Independently execute programming tasks of medium to high complexity with accuracy and timeliness.
  • QC NONMEM datasets and develop automated test suites for R packages used in pharmacometrics workflows.
  • Collaborate with Data Management, Biostatistics, Statistical Programming, and Bioanalytical groups to resolve data issues.

Skills

R programming
NONMEM datasets
PK/PD datasets
QC automation
SDTM/ADaM

Education

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

Tools

NONMEM
R packages

Job description

IQVIA LLC in Reading, United Kingdom, seeks an experienced PK/PD Statistical Programmer to join our pharmacometrics team. You will program, validate, and deliver NONMEM-ready PK/PD datasets based on SDTM/ADaM standards using advanced R skills, ensuring accuracy from unclean to post‑lock clinical data.

The role requires 6+ years in clinical data analysis or pharmacometrics, expert R proficiency, and hands-on NONMEM dataset creation.

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