Global Regulatory Diagnostics Lead - Precision Medicine

Global Regulatory Diagnostics Lead - Precision Medicine

Full-Time 80000 - 100000 £ / year (est.) No working from home possible
Novartis

At a Glance

  • Tasks: Design global regulatory strategies and lead submissions for precision diagnostics.
  • Company: Join Novartis, a leader in innovative healthcare solutions.
  • Benefits: Competitive salary, health benefits, and opportunities for professional growth.
  • Other info: Dynamic role with opportunities to shape the future of healthcare.
  • Why this job: Make a real impact in precision medicine and collaborate with global teams.
  • Qualifications: Experience in regulatory affairs and strong communication skills.

The predicted salary is between 80000 - 100000 £ per year.

Novartis is seeking an experienced Regulatory Diagnostics Associate Director in London.

You will design global regulatory strategies for precision and companion diagnostics, and lead submissions across the product lifecycle, coordinating with cross‑functional teams to enable timely authorisations.

The role involves collaboration with global regulatory teams, preparing briefing documents, and driving regulator interactions.

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Global Regulatory Diagnostics Lead - Precision Medicine employer: Novartis

At Novartis, we pride ourselves on being an exceptional employer that fosters a collaborative and innovative work culture. Our hybrid work model allows for flexibility while providing ample opportunities for professional growth and development in the pharmaceutical industry. With a commitment to enhancing customer experiences for healthcare professionals and patients alike, joining our team means contributing to meaningful work that makes a difference in people's lives.

Novartis

Contact Details:

Novartis Recruitment Team

We think you need these skills to ace Global Regulatory Diagnostics Lead - Precision Medicine

Regulatory Strategy Development
Precision Medicine Knowledge
Companion Diagnostics Expertise
Submission Management
Cross-Functional Team Coordination
Briefing Document Preparation
Regulator Interaction