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Senior Manager Informed Consent

United Kingdom, Uxbridge · Job Posted February 18, 2026
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Job Description

Shape how patients around the world understand and engage with clinical research, leading the delivery of compliant, high-quality informed consent at global scale.

Job Responsibility

  • Lead and develop a high-performing global Informed Consent Form (ICF) team
  • Own the end-to-end ICF development process, driving continuous improvement in quality, speed, and standardisation
  • Provide strategic and operational leadership for ICF planning, resourcing, and execution across the pipeline
  • Ensure compliance with global and country-specific regulatory requirements and inspection readiness
  • Partner cross-functionally to deliver patient-centric, clear, and consistent informed consent content
  • Monitor performance metrics, trends, and inspection findings to drive data-led improvements
  • Act as a change leader, strengthening collaboration, accountability, and clarity of roles across stakeholders
  • Line manage and mentor ICF managers, building capability, engagement, and a culture of excellence

Requirements

  • Degree educated
  • Clinical trial execution experience
  • Previous people leadership managing teams, projects, or resources
  • Previous experience in life sciences including managing data on biopharmaceutical clinical research experience
  • Experience engaging and working across clinical trial teams in multiple geographies to deliver global clinical trials
  • Experience with managing data collection and oversight with external vendor (CROs, central labs, imaging vendors, etc.)
  • Experience in roles that include patient centricity and/or Informed Consent Development and oversight

What we offer

  • Vast opportunities to learn and move up and across our global organization
  • Diverse and inclusive community of belonging
  • Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

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