Hybrid Global Regulatory Submissions Lead (CTA/CTR)

Novartis AG

Greater London

Hybride

GBP 68 000 - 126 000

Plein temps

Il y a 5 jours
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Résumé du poste

Novartis AG in London is seeking a CTA/CTR Team Lead to steer a global regulatory team responsible for high-quality clinical trial submissions and approvals. You will blend people leadership with regulatory expertise to deliver timely outcomes and drive smarter ways of working through simplification and automation.

Based in London with hybrid/remote options for UK-based candidates, the role requires strong regulatory knowledge and international collaboration across teams.

Qualifications

  • Bachelor’s or Master’s degree in a science-related discipline, with regulatory experience.
  • Substantial knowledge of global regulations and processes supporting regulatory clinical trial activities.
  • Experience leading regulatory professionals with people management capabilities.
  • Experience in strategic planning, regulatory review, compliance, submissions and execution.
  • Ability to drive process improvement, simplification, automation and operational excellence.
  • Strong communication and cross-functional collaboration in international environments.

Responsabilités

  • Lead and develop a global regulatory team delivering submissions and approvals.
  • Coach and support team members for growth.
  • Allocate resources across the portfolio balancing priorities.
  • Drive process improvement, simplification and automation.
  • Build relationships with stakeholders and act on feedback.
  • Foster collaboration across Regulatory Affairs and global teams.
  • Champion Novartis culture and behaviours.

Connaissances

People management
Regulatory submissions
Strategic planning
Regulatory compliance
Cross-functional collaboration
Communication skills
Influencing
Problem solving

Formation

Bachelor’s/Master’s in science

Description du poste

Novartis AG in London is seeking a CTA/CTR Team Lead to steer a global regulatory team responsible for high-quality clinical trial submissions and approvals. You will blend people leadership with regulatory expertise to deliver timely outcomes and drive smarter ways of working through simplification and automation.

Based in London with hybrid/remote options for UK-based candidates, the role requires strong regulatory knowledge and international collaboration across teams.

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