Global Regulatory Strategy Team Lead/Sr. Director (Atlanta, GA)
Join to apply for the Global Regulatory Strategy Team Lead/Sr. Director (Atlanta, GA) role at UCB
Global Regulatory Strategy Team Lead/Sr. Director (Atlanta, GA)
Join to apply for the Global Regulatory Strategy Team Lead/Sr. Director (Atlanta, GA) role at UCB
Make your mark for patients
We are seeking a
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
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)
- 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
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 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 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.
Seniority level
Seniority level
Director
Employment type
Employment type
Full-time
Job function
Job function
ResearchIndustries
Pharmaceutical Manufacturing
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