Senior Programming Associate

3 weeks ago


Copenhagen, Copenhagen, Denmark Genmab Full time
Job Summary

Data plays a crucial role in Genmab's innovative cancer treatment process. As a Senior Programming Associate, you will be instrumental in ensuring the accuracy and integrity of data, working closely with cross-functional teams to drive business outcomes. Your expertise in SAS programming and analytical skills will be essential in delivering high-quality data summaries and analysis datasets.

Key Responsibilities

Data Standards and Integrity: Establish and maintain Genmab's SDTM and ADaM database standards, ensuring consistency and adherence to regulatory guidelines.
Data Quality Assurance: Perform database standards consistency checks on databases delivered by vendors, producing other in-house checks of data consistencies.
Programming and Development: Write efficient, well-documented SAS programs to support data analysis, ensure QC before formal release, and produce in-house preparation for DMC-meetings, RP2D-selection preparations, and supplementary material for interim analysis and final analyses.
Collaboration and Communication: Work closely with Data Management, Statistics, Drug Safety, Medical, Clinical Pharmacology, and Biomarker functions, providing feedback on application development and contributing to process improvements.

Requirements

Programming Expertise: Proficient in SAS software package and other programming languages (R and Python).
Education: Minimum Bachelor of Science degree or equivalent qualifications.
Language: Proficient in both written and spoken English.
Experience: At least 2 years of experience within the pharmaceutical industry as a Programmer (for Senior Programming Associate level).

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