Global Regulatory Affairs Associate Director (cardio-metabolic)

Novartis

London, United Kingdom
Hybrid
Significant experience in regulatory affairs
Proven track record in project management
Strong knowledge of clinical trials
The role involves directing the development and submission of regulatory documents

Job Summary

  • The role involves directing the development and submission of regulatory documents.
  • It ensures timely approval and compliance of new and marketed products.
  • The position serves as a regulatory liaison throughout the product lifecycle.

Matching Summary

The role involves directing the development and submission of regulatory documents.

Skills & Requirements

Must-have

  • Significant experience in regulatory affairs
  • Proven track record in project management
  • Strong knowledge of clinical trials

Nice-to-have

  • Excellent problem-solving skills
  • Ability to navigate Health Authority interactions
  • Experience in cross-functional settings

Key Requirements

  • Bachelor’s or Master’s degree in Life Sciences
  • Experience representing the organization
  • Fluency in English is essential

Work Rights

Not specified

Tailored Resume

Cover Letter