Global Regulatory Strategy Team Lead Neurology (UK)
Join to apply for the Global Regulatory Strategy Team Lead Neurology (UK) role at UCB
Global Regulatory Strategy Team Lead Neurology (UK)
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We are looking for a Global Regulatory Strategy Team Lead Neurologyto 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 Neurologyprovides senior leadership, mentorship and oversight for the Global Regulatory Leads within the appointed therapeutic area. The role also foresees Global Regulatory Lead project responsibility.
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:
* 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
Seniority level
* Seniority level
Director
Employment type
* Employment type
Full-time
Job function
* Job function
Research
* Industries
Biotechnology Research and Pharmaceutical Manufacturing
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