Regulatory Stakeholders Head neurodegeneration at UCB
Slough, England, United Kingdom -
Full Time


Start Date

Immediate

Expiry Date

12 Sep, 25

Salary

0.0

Posted On

13 Jun, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Management Skills, Clinical Development

Industry

Pharmaceuticals

Description

MAKE YOUR MARK FOR PATIENTS

We are looking for a Regulatory Stakeholders Head Neurodegeneration who is passionate about clinical development, is a strategic thinker, and a collaborative and inclusive leader to join us in our patient evidence organisation, based in our headquarters in Brussels, Belgium; in Slough, UK or in Raleigh, US.

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.

Responsibilities

ABOUT THE ROLE

You will be working as a core member of the neurodegeneration asset team that oversees and manages product development strategy in a number of neurodegenerative conditions. You will lead the Regulatory Stakeholder Sub-team and serve as the primary representative for Regulatory, Technical, and Clinical Development within the Asset Leadership Team, ensuring clinical and regulatory delivery across all development phases.

WHAT YOU’LL DO

  • Lead the Regulatory Stakeholder Sub-team, including members from Patient Evidence and Patient Solutions
  • Deliver the Asset Strategic Development Plan and design clinical development programs
  • Ensure technical, regulatory, and CMC strategies reflect global and regional considerations
  • Oversee clinical evidence generation and guide the design of evidence generation studies
  • Develop and deliver competitive Regulatory and Clinical Strategic Plans
  • Provide clinical and medical oversight of the clinical program

INTERESTED? FOR THIS ROLE WE’RE LOOKING FOR THE FOLLOWING EDUCATION, EXPERIENCE, AND SKILLS

  • Master’s or PhD in a scientific/medical field
  • Minimum of 15 years of pharmaceutical industry experience, with 12+ years in regulatory and/or clinical development
  • Proven experience in submission and approval of NDA/BLA/MAA
  • Deep understanding of neurodegeneration therapeutic area
  • Strong strategic decision-making and risk management skills
  • Excellent communication and stakeholder engagement abilities
    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!
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