Rbqm Specialist

Novo Nordisk AS

Søborg, Denmark
On-site
Rbqm knowledge expert
Process manager for protocol deviations
Corporate process content responsibility
Novo Nordisk is seeking an RBQM Specialist to manage Protocol Deviations and Issue Management processes within their Clinical Risk Management and Oversight department, emphasizing patient safety and trial quality. The role requires a strong background in clinical trial management, RBQM processes, and experience in the pharmaceutical industry

Job Summary

  • Act as a Subject Matter Expert and Process Responsible for e.g. Protocol Deviations and Issue Management process.
  • The team owns and continuously improves enterprise‑level RBQM processes, providing expert oversight of protocol deviations and issue management across clinical programs.
  • When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.

Matching Summary

Match Score: 85

Novo Nordisk is seeking an RBQM Specialist to manage Protocol Deviations and Issue Management processes within their Clinical Risk Management and Oversight department, emphasizing patient safety and trial quality. The role requires a strong background in clinical trial management, RBQM processes, and experience in the pharmaceutical industry.

Skills & Requirements

Must-have

  • RBQM knowledge expert
  • Process Manager for Protocol Deviations
  • Corporate process content responsibility
  • Develop corporate training material
  • Global oversight of RBQM processes

Nice-to-have

  • Strong integrity and ethical judgment
  • Team-oriented and collaborative
  • Adaptable to evolving settings
  • Focus on patient safety and product quality

Key Requirements

  • Master’s degree in natural sciences or similar
  • Minimum 5 years of relevant practical experience
  • Experience with GxP processes, inspections, deviations, and issue management
  • Fluent in written and verbal English

Work Rights

Not specified

Tailored Resume

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