Senior Immunology Benefit-Risk & Safety Lead (Hybrid)

UCB S.A.

Reading

Hybrid

GBP 80.000 - 120.000

Vollzeit

14 Tage+

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Zusammenfassung

UCB S.A. is seeking a senior safety professional to develop and maintain benefit-risk assessments and risk management approaches across clinical development.

You will analyze diverse evidence to identify emerging risks and communicate their potential impact on patients, and prepare regulatory safety responses and submission documents. Collaboration across scientific, medical and regulatory functions is essential to turning complex evidence into practical decisions.

Qualifikationen

  • Experience in pharmaceutical clinical development and medical safety.
  • Proven ability to produce high-quality safety outputs and regulatory documents.
  • Senior profiles should lead strategic safety deliverables and program safety leadership.
  • Ability to communicate complex evidence in English, written and spoken.

Aufgaben

  • Develop and maintain benefit-risk assessments and risk management approaches across clinical development.
  • Analyze diverse scientific and safety evidence to identify emerging risks and their patient impact.
  • Prepare safety reports, regulatory responses, and submission documents.
  • Collaborate across scientific, medical and regulatory functions to translate evidence into decisions.
  • At senior levels, own benefit-risk strategy and lead governance discussions, coordinating work across functions.

Kenntnisse

Clinical safety
Benefit-risk assessment
Safety writing
Risk management
Cross-functional collaboration
English communication

Ausbildung

Bachelor's/Master's in a relevant scientific field
MD/PhD desirable

Jobbeschreibung

UCB S.A. is seeking a senior safety professional to develop and maintain benefit-risk assessments and risk management approaches across clinical development.

You will analyze diverse evidence to identify emerging risks and communicate their potential impact on patients, and prepare regulatory safety responses and submission documents. Collaboration across scientific, medical and regulatory functions is essential to turning complex evidence into practical decisions.

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