Senior Safety Scientist / Associate Director / Director

Roche

Welwyn, United Kingdom
Hybrid
Qualified healthcare professional or life sciences graduate
Proven drug safety and clinical development experience
Understanding of gxp and regulated processes
Roche is seeking a Senior Safety Scientist/Associate Director/Director for their Welwyn, UK office, offering a hybrid work environment. The role focuses on safety science and pharmacovigilance across Roche's portfolio, requiring a qualified healthcare professional with expertise in drug safety and clinical development

Job Summary

  • The position provides hands-on safety science and pharmacovigilance support to molecules across the Roche portfolio.
  • Responsibilities include signal detection, benefit-risk assessment, and contributing to regulatory authority submissions such as NDAs and MAAs.
  • Roche fosters a culture of personal expression, open dialogue, and genuine connections where every voice matters.

Matching Summary

Match Score: 85

Roche is seeking a Senior Safety Scientist/Associate Director/Director for their Welwyn, UK office, offering a hybrid work environment. The role focuses on safety science and pharmacovigilance across Roche's portfolio, requiring a qualified healthcare professional with expertise in drug safety and clinical development.

Skills & Requirements

Must-have

  • Qualified healthcare professional or Life Sciences graduate
  • Proven drug safety and clinical development experience
  • Understanding of GxP and regulated processes
  • Experience with ICSR case management and aggregate reporting
  • Strong orientation towards process improvement

Nice-to-have

  • Postgraduate qualification in Life sciences or Medical field
  • Excellent communication skills both written and verbal
  • Ability to train others on departmental practices
  • Understanding of project management methodology
  • Experience working with remote global partners

Key Requirements

  • Minimum: Qualified healthcare professional or Life Sciences graduate
  • Preferred: Postgraduate qualification (PhD/MSc) or Medical qualification
  • Proven experience in pharmaceutical industry drug safety
  • Knowledge of GxP and end-to-end clinical trial lifecycle

Work Rights

Not specified

Tailored Resume

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