Senior Standards Developer

Senior Standards Developer to enable high-quality clinical data and data standards development at Novo Nordisk, shaping the design, governance, and utilisation of clinical data standards for global development programmes.

Requirements

• Master's or Bachelor's degree in natural/life sciences, medicine, pharmacy, computer science, or similar
• Minimum 4 years of experience in clinical trial conduct and/or clinical data standards governance, preferably within the pharmaceutical industry
• Experience within clinical data management, trial management, or statistical programming, with sound knowledge of data flows and systems supporting clinical data collection and processing
• Strong knowledge of specific tools and programming languages (SAS, Python, R...)
• Solid understanding of CDISC standards, SDTM, Controlled Terminology (CT)
• Strong communication and stakeholder management capabilities, with the ability to navigate diverse viewpoints and drive alignment
• A proactive mindset, high quality orientation, cultural awareness, and the ability to manage a variable workload

Benefits

• Learning and development opportunities
• Career-focused benefits
• Diverse and inclusive work environment