Associate Director, Clinical Pharmacology Data Programming Specialist

Role: Associate Director, Clinical Pharmacology Data Programming Specialist, leading data programming and QC activities supporting clinical pharmacology and pharmacometric analyses within Genmab's development portfolio. Responsibilities: program analysis datasets and outputs for PK, PK/PD, exposure-response, NCA, modeling, and biomarkers; develop validation strategies, automate workflows, and support regulatory submissions; collaborate cross-functionally with pharmacologists, statisticians, data management, and external vendors; contribute to standards and automation initiatives. Requirements: Master's in Statistics, Biostatistics, Computer Science, or related field; extensive programming experience in R and/or SAS with clinical trial data; knowledge of SDTM, ADaM, CDISC standards; experience supporting pharmacometric analyses (PK/PD, population PK); familiarity with NONMEM and related tools preferred; 5+ years in biotech/pharma. HighValue: clinical pharmacology, pharmacometrics, PK/PD modeling, regulatory submission support, analysis dataset QC, automation, validation, cross-functional collaboration. WorkSetup: flexible remote work (20%-40%); some team interactions required.