Informed Consent Manager
Informed Consent Manager
United Kingdom - Uxbridge APLICAR AHORAHOW MIGHT YOU DEFY IMAGINATION?
If you feel likeyou’repart of something bigger,it’sbecause you are. AtAmgenour 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,manufacturingand delivering ever-better products that reachover10 million patientsworldwide.It’stime for a career you can be proud of. Join us.
INFORMED CONSENT MANAGER
LIVE
What you will do
In this vitalroleyou 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.
The responsibilities of the role will include:
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 ensureaccuratealignment 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 tomaintainspeed 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.
Identifyand implement practical improvements to ICF processes, tools, and ways of working to improve delivery performance.
WIN
What we expect of you
We are all different, yet we all use our unique contributions to serve patients.What weseekin you as anexperienced professional, are these qualifications and skills:
Degree educated
Clinical trial execution experience andexperience working within a global team structureas well asproject management experience
Previousexperience in life sciences or a related field, including biopharmaceutical clinical research.
Experience in authoring ICF forms and in a clinicalsettinge.g.clinicalsiteroleis preferred.
THRIVE
What you can expect of us
As we work to develop treatments that take care ofothers, sowe work to care for our teammates’ professional and personal growth and well-being.
Vast opportunitiestolearnand 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
LOCATION:Ability to work flexibly from home with regular office work either from our Cambridge or Uxbridge next generation workspace.
APPLY NOW
for a career that defies imagination
In our quest to serve patientsabove all else, Amgen is the first to imagine, and the last to doubt. Join us.
careers.amgen.com
Equal Opportunity Statement
Amgen 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.
We will ensure that individuals with disabilities are provideda reasonableaccommodation toparticipatein the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to requestan accommodation.