Clinical Process Manager: Deliver Excellence in Quality Assurance
5 days ago
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We are seeking a highly skilled Senior GCP Advisor to join our Clinical QMS department. As a key member of the team, you will be responsible for ensuring compliance with GCP and regulatory requirements.
The successful candidate will have at least 8 years of experience in clinical research and drug development, as well as a strong knowledge of GCP and other relevant regulations.
You will be expected to manage updates to our standard operating procedures (SOPs), verify and approve SOPs, and ensure global consistency and compliance in clinical development processes.
The ideal candidate will possess excellent communication and presentation skills, be able to collaborate effectively with cross-functional teams and stakeholders, and have a proactive mindset with a focus on continuous quality improvement.
About the Department:
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The Clinical Quality Management System (QMS) department is part of R&D Quality at Novo Nordisk. We play a vital role in supporting the drug development process to ensure high-quality processes and procedures.
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