Senior Manager Informed Consent
Senior Manager Informed Consent
United Kingdom - Uxbridge Apply NowHOW 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.
SENIOR MANAGER INFORMED CONSENT
LIVE
What youwill do
In this vital role youshape how patients around the world understand and engage with clinical research,leadingthe delivery of compliant, high-quality informedconsent atglobal scale.
The responsibilities of the role will include:
Lead and develop a high-performing global Informed Consent Form (ICF) team, ensuring high quality, compliance, andtimelydelivery across all portfolios.
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.
Linemanageand mentor ICF managers, building capability, engagement, and a culture of excellence.
WIN
What we expectofyou
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 andpreviouspeopleleadership managing teams, projects, or resources.
Previousexperience in life sciencesincluding managing data on biopharmaceutical clinical research experience.
Experience engaging and working across clinical trial teams in multiple geographies to deliver global clinical trials.
Experience withmanaging data collection and oversight with externalvendor(CROs, central labs, imaging vendors, etc.).
Experienceinroles that include patient centricity and/or Informed Consent Development and oversight
THRIVE
What you can expectofus
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.
