Global Regulatory Strategy Team Lead Neurology (UK) - #144260

Make your mark for patients

We are looking for a Global Regulatory Strategy Team Lead Neurology to join us in our Global Regulatory Affairs team, based in any of our Brussels (Belgium), Slough (UK) or Atlanta or Raleigh (US) offices.

About The Role

The Global Regulatory Strategy Team Lead Neurology provides senior leadership, mentorship and oversight for the Global Regulatory Leads within the appointed therapeutic area. .

Who You’ll Work With

You will report to the Head of Global Regulatory Strategy

What You’ll Do

• Be responsible for providing leadership and management for the Global Regulatory Leads within the therapeutic area and cross- functional stakeholders
• Provide strategic regulatory oversight and lead the regulatory strategy teams on assigned project(s)
• Drive a culture of accountability and excellence and promote drug development leadership
• Motivate employees to perform at their highest ability
• Accountable for ensuring that governance meeting outcomes are appropriately communicated
• As a member of the Global Regulatory Strategy Leadership Team, provide overall strategic direction to the Global Regulatory Strategy organisation and contribute to Global Regulatory Affairs and cross-organisational improvement initiatives
• Oversee general Global Regulatory Lead training and development, create consistency by ensuring best practices and learnings are shared across therapeutic areas/products
• Recruit, develop, and retain highly talented and skilled Global Regulatory Leads that are ready to take on tomorrow’s challenges
  
  

Interested? For this position you’ll need the following education, experience and skills:

• Bachelor’s degree required, master’s preferred
• Significant pharmaceutical industry experience inclusive of several years of regulatory experience, knowledge of neurology therapeutic area preferred
• Highly driven and seasoned leader with line management as well as matrix experience
• Global regulatory experience for core countries (US, EU) required and Japan and China preferred, with a proven track record of significant regulatory accomplishments
• Thorough understanding of drug development process and global regulatory requirements and processes
• Up to date knowledge of the global regulatory environment, good understanding of the complex set of regulations within which the organization operates and awareness of the subtleties of regulations worldwide
  
  

Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About Us

UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 8,500 people in all four corners of the globe, inspired by patients and driven by science.

Why work with us?

At UCB, we don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equal opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.

UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on [email protected] . Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.