Quality
GCP Advisor Specialist, Clinical QA, Søborg, Denmark
Opportunity summary
Official occupation: Apoteker. Employment conditions: Almindelige vilkår. Employer CVR: 24256790.
Primary career market
Health & Life Science (reviewed employer registry). Are you passionate about quality, compliance, and driving excellence in clinical development? Do you thrive in a global environment where you can influence processes, advise senior stakeholders, and help shape the future of quality across clinical research?
Join Novo Nordisk as a GCP Advisor Specialist and play a pivotal role in ensuring compliance, continuous improvement, and quality oversight across our worldwide clinical development activities.
Your New Role As a GCP Advisor Specialist within Clinical QA, you will act as a trusted quality partner to the global clinical organisation, providing expert guidance on Good Clinical Practice (GCP), quality management systems, and regulatory expectations.
You will work across functions and geographies to drive consistency, compliance, and continuous improvement, while contributing to a culture of simplicity, agility, and innovation.
Key responsibilities include
- - Providing expert GCP advice and quality guidance to stakeholders across global clinical development.
- - Leading and participating in cross-functional improvement initiatives and projects to strengthen quality and compliance.
- - Perform vendor assessments1 …
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