Senior Programming Associate
3 weeks ago
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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