Global Program Regulatory Manager - Neuroscience

Salary Range:

£39,567.50 - £73,482.50

Job Description Summary

Work Arrangement: Hybrid
Location: London, United Kingdom
Relocation Support: This role is based in London, United Kingdom. Novartis is unable to offer relocation support: please only apply if accessible.

ABOUT THE ROLE
Drive regulatory execution that enables innovation in neuroscience to reach patients faster. As Regulatory Affairs Manager – Neuroscience, you will play a key role in delivering regulatory strategies across assigned regions, ensuring high-quality submissions and effective interactions with Health Authorities. Working cross-functionally, you will translate complex scientific and clinical data into regulatory deliverables, supporting timely approvals and maintaining compliance throughout the product lifecycle. This role offers the opportunity to build deep regulatory expertise while contributing to impactful global programs in a dynamic and collaborative environment.

Job Description

Key Responsibilities

• Implement regulatory strategy and manage operational activities across assigned regions

• Support development of global regulatory strategy and identify risks or gaps for assigned regions

• Partner with regional teams to align regulatory plans and ensure effective execution

• Lead preparation of Health Authority interactions, including briefing documents and response plans

• Drive coordination and submission of regulatory dossiers across assigned regions

• Review, approve, and submit Clinical Trial Applications and Investigational New Drug applications

• Manage responses to Health Authority queries and support timely approvals while minimising delays

Essential Requirements

• Experience in regulatory affairs within pharmaceutical or biotechnology environments

• Knowledge of regulatory submission processes and compliance requirements

• Experience supporting regulatory strategy and execution across multiple regions

• Strong project management and organisational skills in a matrix environment

• Ability to collaborate with cross-functional teams and external stakeholders

• Strong problem-solving skills and attention to detail in regulatory decision-making

• Effective communication skills and ability to interpret and present technical information clearly

Why Novartis:
Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here:
https://www.novartis.com/about/strategy/people-and-culture

You’ll receive:
You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook.

Commitment to Diversity and Inclusion:

Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Join our Novartis Network:
If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network

Skills Desired

Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance