Global Regulatory Affairs Associate Director (cardio-metabolic)
Novartis UK
London, United Kingdom
Hybrid
Regulatory strategies
Health authority interaction
Regulatory dossier submissions
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.
It also ensures timely approval and compliance of new and marketed products, and serves as a regulatory liaison throughout the product lifecycle.
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 strategies
Health Authority interaction
regulatory dossier submissions
product lifecycle management
pharmaceutical industry experience
Nice-to-have
problem-solving skills
negotiation skills
detail-oriented
cross-functional teams
risk management
Key Requirements
Bachelor's or Master's degree
Significant regulatory affairs experience
Proven project management track record
Experience with clinical trials and drug development