Immunology Safety & Benefit-Risk Strategy Lead

UCB S.A.

Princes Risborough

Híbrido

GBP 80.000 - 110.000

Jornada completa

14 días+

Una candidatura completa en un minuto

Currículum y carta de presentación personalizados, listos para enviar.

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Descripción de la vacante

UCB S.A. in the United Kingdom is seeking an experienced pharmacovigilance professional to develop and maintain benefit-risk assessments across clinical development, safety monitoring and risk management.

You will analyze diverse safety evidence, prepare regulatory responses and decision materials, and collaborate with science, medical and regulatory teams to translate complex data into actionable safety decisions.

Formación

  • Bachelor's/Master's degree in a relevant scientific discipline; a relevant advanced degree is desirable such as an MD/PhD.
  • Experience in pharmaceutical clinical development, medical safety, benefit-risk assessment, safety writing and risk management, appropriate to level.
  • Experience in immunology, CAR-T cell therapy or T-cell engager development is an advantage.
  • Ability to analyse scientific evidence and communicate balanced conclusions clearly in written and spoken English.
  • Experience contributing to safety outputs; senior profiles should demonstrate strategic ownership and leadership of complex deliverables (indication or global program safety leadership).
  • Comfort working across functions, priorities and lifecycle stages while maintaining quality, integrity and patient focus.
  • Interest in roles based in our Belgium or United Kingdom hubs and, openness to an international working environment.

Responsabilidades

  • Develop and maintain benefit-risk assessments, safety monitoring and risk management approaches across clinical development.
  • Analyse diverse scientific and safety evidence to identify emerging risks and explain their potential impact on patients.
  • Prepare clear, accurate safety reports, regulatory responses, submission documents and decision materials.
  • Collaborate across scientific, medical and regulatory functions to turn complex evidence into practical decisions.
  • At senior levels, own benefit-risk strategy, lead governance discussions and coordinate high-quality work across functions.

Conocimientos

Benefit-risk assessment
Safety monitoring
Risk management
Clinical development
Scientific analysis
Written English communication
Cross-functional collaboration
Strategic leadership

Educación

Bachelor's/Master's degree in a relevant scientific discipline
Advanced degree (MD/PhD) desirable

Descripción del empleo

UCB S.A. in the United Kingdom is seeking an experienced pharmacovigilance professional to develop and maintain benefit-risk assessments across clinical development, safety monitoring and risk management.

You will analyze diverse safety evidence, prepare regulatory responses and decision materials, and collaborate with science, medical and regulatory teams to translate complex data into actionable safety decisions.

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