Associate Director, Clinical Pharmacology Data Programming Specialist

At Genmab, we are dedicated to building extra[not]ordinary futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals’ unique contributions are valued and drive innovative solutions to meet the needs of our patients, care partners, families and employees.

Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe that being proudly authentic and determined to be our best is essential to fulfilling our purpose. Yes, our work is incredibly serious and impactful, but we have big ambitions, bring a ton of care to pursuing them, and have a lot of fun while doing so.

Does this inspire you and feel like a fit? Then we would love to have you join us!

The Role The Associate Director, Clinical Pharmacology Data Programming Specialist will provide technical expertise and project leadership for data programming, data management, and quality-control activities supporting clinical pharmacology and pharmacometrics across Genmab’s development portfolio.

The role combines hands-on programming with project coordination, including delivery of high-quality analysis-ready data and quantitative outputs, planning timelines, defining programming and QC approaches, and partnering with clinical pharmacologists, pharmacometricians, Clinical Programming, Data Management, Biostatistics, Bioanalytics, Biomarkers, and external vendors.

Work arrangement:

This role offers flexibility to work away from the office for 20%–40% of a typical schedule. Employees may use this work schedule in increments of single days or multiple consecutive days, provided it does not exceed 40% within a 60-day period, and is approved by the hiring manager.

Key Responsibilities Pharmacometrics and Clinical Pharmacology Programming
· Lead or support programming and QC of analysis-ready datasets and outputs for population PK, exposure-response, PK/PD, NCA, modeling and simulation, immunogenicity, biomarker, and related quantitative analyses.
· Develop, maintain, and QC NONMEM-ready and other pharmacometric analysis datasets.
· Integrate and pool clinical, dosing, PK, PD, immunogenicity, biomarker, efficacy, safety, laboratory, SDTM, ADaM, and other relevant data across studies.
· Develop and maintain programming specifications, derivation rules, analysis datasets, tables, figures, listings, and exploratory outputs.
· Provide programming support for data-driven analyses, health-authority requests, publications, conference presentations, and other CPQS deliverables.

Programming Quality Control and Validation
· Perform independent QC of analysis datasets, derivations, programs, tables, figures, listings, and other quantitative outputs using a developer-reviewer model where appropriate.
· Develop validation plans and QC strategies based on the intended use and regulatory importance of the analysis.
· Design, test, validate, and document programming logic and reusable analytical workflows, ensuring traceability, reproducibility, and appropriate version control.
· Develop automated and reusable data checks and QC tools to improve consistency and efficiency.

Project Coordination and Delivery
· Plan and coordinate programming activities, milestones, and deliverables across one or more development programs in alignment with project and regulatory timelines.
· Work with CPQS scientists to define data and programming requirements and identify risks related to scope, data availability, timelines, or deliverables.
· Prioritize requests and support rapid-turnaround and ad hoc analyses when required.
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