Associate Director, Clinical Pharmacology Data Programming Specialist

Genmab

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Clinical OperationsFull timeCompany career page

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Role summary

Genmab seeks an Associate Director of Clinical Pharmacology Data Programming to lead technical programming and data management activities supporting pharmacometrics and clinical pharmacology across its development portfolio. The role combines hands-on programming expertise with project coordination, including dataset preparation, quality control, and regulatory submission support.

Where this listing comes from

This listing was compiled by RoleLantern from the employer's publicly available posting on Phenom, captured and rephrased by RoleLantern using automated (AI) tools on 2026-10-04 (originally posted 2026-10-02). It was not submitted or confirmed by the employer through RoleLantern. Details may be inaccurate, incomplete, outdated, or no longer available; please confirm with the employer's official posting before applying.

What they're looking for

Master's degree in Statistics, Biostatistics, Computer Science, Mathematics, Engineering, or related quantitative discipline
Substantial programming experience in biotechnology, pharmaceutical, or clinical development settings
Strong experience with clinical trial data and analysis-ready dataset development
Proficiency in programming languages commonly used in pharmacometrics and clinical analysis
Knowledge of NONMEM, pharmacometric workflows, and quantitative analysis standards
Experience with regulatory submissions and health-authority interactions
Project management and cross-functional collaboration skills

What you'll be doing

Lead programming and quality control of analysis-ready datasets for population PK, exposure-response, and related pharmacometric analyses
Develop and maintain NONMEM-ready datasets and pharmacometric analysis specifications with independent QC
Plan and coordinate programming activities, milestones, and deliverables across development programs aligned with regulatory timelines
Support clinical pharmacology components of regulatory submissions, including BLA and global submission preparation
Contribute to development of programming standards, reusable workflows, and automation tools to improve efficiency and consistency

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Date posted2 days ago

Last source checkToday

Salary listedNeeds clarity

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