Make your mark for patients

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

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 organization and contribute to Global Regulatory Affairs and cross-organizational 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:
Minimum qualifications:
• Bachelor’s degree
• Minimum of 15 years of regulatory experience in the pharmaceutical industry
• Minimum of 5 years management/leadership experience
• Minimum of 5 years regulatory experience for core countries (US, EU)
Preferred qualifications:
• Master’s degree
• Knowledge of the neurology therapeutic area
• Regulatory experience with Japan and China
• 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

Internal applicants should be in their current job for at least 12 months, must meet performance standards and are not on formal corrective/disciplinary process (PIP), warning, final warning, or compliance warning letters within the last 12 months. Please inform your Manager or your Talent Partner before applying to any internal job opportunities.

UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable federal, state, or local law. UCB invites you to voluntarily self-identify during the application process. Provision of self-identification information is entirely voluntary and a decision to provide or not provide such information will not have any effect on your application for employment, your employment with UCB, or otherwise subject you to any adverse treatment. Any information you provide will be considered confidential and will be kept separate from your application and/or personnel file and will only be used in accordance with applicable laws, orders, and regulations.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on US-Reasonable_Accommodation@ucb.com for application to US based roles. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.

Requisition ID: 90487

Recruiter: Kevin Ross

Hiring Manager: Tom Meeusen

Talent Partner: Bianca Hinshaw

Job Level: SM I

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