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Informed Consent Manager
<p>HOW MIGHT YOU DEFY IMAGINATION?If you feel like you\'re part of something bigger, it\'s because you are. At Amgen our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world\'s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing and delivering ever-better products that reach over 10 million patients worldwide. It\'s time for a career you can be proud of. Join us.</p><p>INFORMED CONSENTMANAGERWhat you will doIn 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.</p><p>The responsibilities of the role will include:</p><p>Manage the end-to-end delivery of study-specific informed consent forms (ICFs), ensuring they are high quality, compliant, and delivered on time.</p><p>Review, edit, and contribute directly to ICF content to ensure accurate alignment with study protocols and regulatory requirements.</p><p>Work day-to-day with Study Delivery Teams and ICF Authors to develop ICFs that meet study timelines and operational needs.</p><p>Perform quality checks on all study-level ICFs, resolving issues quickly to maintain speed and consistency.</p><p>Partner with Patient Engagement teams to incorporate patient feedback and improve clarity, accessibility, and usability of ICFs.</p><p>Coordinate ICF translations, version control, and country-specific updates to support global study execution.</p><p>Maintain and actively manage study ICF tracking, reconciliation, and status reporting across studies.</p><p>Identify and implement practical improvements to ICF processes, tools, and ways of working to improve delivery performance.</p><p>WINWhat we expect of youWe are all different, yet we all use our unique contributions to serve patients. What we seek in you as an experienced professional, are these qualifications and skills:</p><p>Degree educated</p><p>Clinical trial execution experience and experience working within a global team structure as well as project management experience.</p><p>Previous experience in life sciences or a related field, including biopharmaceutical clinical research.</p><p>Experience in authoring ICF forms and in a clinical setting, e.g., clinical site role is preferred.</p><p>THRIVEWhat you can expect of usAs we work to develop treatments that take care of others, so we work to care for our teammates\' professional and personal growth and well-being.</p><p>Vast opportunities to learn and move up and across our global organization.</p><p>Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act.</p><p>Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits.</p><p>LOCATIONAbility to work flexibly from home with regular office work either from our Cambridge or Uxbridge next generation workspace.</p><p>APPLY NOWfor a career that defies imaginationIn our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us.</p><p>careers.amgen.comEqual Opportunity StatementAmgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.</p><p>We will ensure that individuals with disabilities are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation.</p><p>#J-18808-Ljbffr</p> Salary: GBP 36000 - 60000 per year