Global Regulatory Strategy Team Lead Neurology (Raleigh (US) Position Available In Wake, North Carolina

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 I nterested? 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 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 laws. Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on EMEA-Reasonable_Accommodation@ucb.com . 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 Please consult HRAnswers for more information on job levels.