Global Regulatory Affairs Associate Director (cardio-metabolic)
Novartis
London, United Kingdom
Hybrid
Regulatory strategy implementation
Health authority interaction
Regulatory dossier submission
The role involves directing the development and submission of regulatory documents, providing strategic direction and negotiating with agencies to expedite approvals
Job Summary
The role involves directing the development and submission of regulatory documents, providing strategic direction and negotiating with agencies to expedite approvals.
Lead the implementation of regulatory strategies and operational activities across major global regions while ensuring timely and compliant responses to Health Authority queries.
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Matching Summary
The role involves directing the development and submission of regulatory documents, providing strategic direction and negotiating with agencies to expedite approvals.
Skills & Requirements
Must-have
Regulatory strategy implementation
Health Authority interaction
Regulatory dossier submission
Cross-functional team collaboration
Regulatory compliance management
Risk management in regulatory affairs
Nice-to-have
Negotiation skills
Problem solving skills
Detail-oriented
Experience in cross-cultural settings
Strategic planning input
Key Requirements
Bachelor’s or Master’s degree in Life Sciences or related field