Global Regulatory Strategy Team Lead Neurology (Belgium) (90485)
Global Regulatory Strategy Team Lead Neurology (Belgium) (90485)
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Job Description
Make your mark for patients
We are looking for aGlobal Regulatory Strategy Team Lead Neurologyto join us in ourGlobal Regulatory Affairsteam 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 youll work with
You will report to the Head of Global Regulatory Strategy
What youll 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 tomorrows challenges
Interested For this position youll need the following education experience and skills:
- Bachelors degree required masters 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
If you are interested to learn more about R&D within UCB please find more information hereR&D at UCB.
RANDATUCB
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 8500 people in all four corners of the globe inspired by patients and driven by science.
Why work with us
At UCB we dont just complete tasks we create value. We arent 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 thats 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 . Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.
Required Experience:
Exec
Employment Type
Full Time
