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GCP Advisor Specialist

The position

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In close collaboration with your colleagues in R&D Quality, you will ensure that Novo Nordisk is in compliance with GCP and other relevant external and internal requirements in an optimal way without putting unnecessary burden on the organisation. The different positions cover a range of quality and compliance tasks including:
• being responsible for developing and maintaining our quality management system, with a strong focus on GCP and compliance globally. 
• providing GCP support to stakeholders globally, 
• being a Quality Partner for our stakeholders
• be the quality support and partner for a Phase 1 unit in Denmark

You will be part of a dynamic area, where the positions offer high impact, and where you are expected to take great ownership and responsibility to setting the right quality bar in the global organisation. 

Qualifications
You have a degree in pharmacy, medicine, science or similar and a strong command of written and spoken English. You have at least 10 years of experience in clinical research and drug development, as well as solid knowledge of GCP and other relevant regulations. Experience within clinical quality assurance, project management, trial management/monitoring, Phase 1 trials or GCP Audit is required.

You take a positive and pragmatic approach to problem solving and you are eager to optimise and simplify processes around you. You are proactive, courageous and have strong communication and interpersonal skills. You are organised, detail-oriented without losing the big picture and quality-conscious as well as curious by nature. You are a team player and you thrive working across departments in an international organisation.


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