Gcp Advisor Specialist

Novo Nordisk AS

Søborg, Capital Region of Denmark, DK
On-site
Gcp advice and support
Global consistency and compliance
Lead sponsor inspections
Novo Nordisk is seeking a GCP Advisor Specialist to join their Clinical Compliance and Inspections team in Søborg, Denmark. The ideal candidate will have extensive experience in clinical research and drug development, with a strong focus on GCP compliance and quality improvement

Job Summary

  • This position is designed for an expert specialist who operates with confidence and independence, brings deep subject matter expertise, and navigates complex, high‑impact tasks across the area.
  • Clinical Compliance and Inspections plays a critical role in safeguarding the quality, integrity, and regulatory compliance of clinical trial activities.
  • 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 a GCP Advisor Specialist to join their Clinical Compliance and Inspections team in Søborg, Denmark. The ideal candidate will have extensive experience in clinical research and drug development, with a strong focus on GCP compliance and quality improvement.

Skills & Requirements

Must-have

  • GCP advice and support
  • global consistency and compliance
  • lead sponsor inspections
  • global inspection readiness process
  • quality by design
  • cross-functional initiatives

Nice-to-have

  • positive and pragmatic approach
  • process improvement, simplicity, agility, and innovation
  • strategic mindset
  • collaborative team player

Key Requirements

  • Degree in medical, biological, or pharmaceutical sciences
  • At least 7 years of experience in clinical research
  • Detailed knowledge of GCP and global regulatory requirements
  • Experience with global collaboration
  • Fluency in English (written and verbal)
  • Sound IT skills, including proficiency in Microsoft Office

Work Rights

Not specified

Tailored Resume

Cover Letter