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Informed Consent Manager

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

In this vital role you will help bring innovative medicines to patients by delivering high-quality, patient-centric informed consent forms that support the successful execution of global clinical studies.

Job Responsibility

  • Manage the end-to-end delivery of study-specific informed consent forms (ICFs), ensuring they are high quality, compliant, and delivered on time
  • Review, edit, and contribute directly to ICF content to ensure accurate alignment with study protocols and regulatory requirements
  • Work day-to-day with Study Delivery Teams and ICF Authors to develop ICFs that meet study timelines and operational needs
  • Perform quality checks on all study-level ICFs, resolving issues quickly to maintain speed and consistency
  • Partner with Patient Engagement teams to incorporate patient feedback and improve clarity, accessibility, and usability of ICFs
  • Coordinate ICF translations, version control, and country-specific updates to support global study execution
  • Maintain and actively manage study ICF tracking, reconciliation, and status reporting across studies
  • Identify and implement practical improvements to ICF processes, tools, and ways of working to improve delivery performance

Requirements

  • Degree educated
  • Clinical trial execution experience
  • Experience working within a global team structure
  • Project management experience
  • Previous experience in life sciences or a related field, including biopharmaceutical clinical research
  • Experience in authoring ICF forms
  • Experience in a clinical setting e.g. clinical site role is preferred

What we offer

  • Vast opportunities to learn and move up and across our global organization
  • Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
  • Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

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