Senior Manager Informed Consent

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.  

SENIOR MANAGER INFORMED CONSENT 

LIVE 

What you will do 

In this vital role you shape how patients around the world understand and engage with clinical research, leading the delivery of compliant, high-quality informed consent at global scale. 

The responsibilities of the role will include: 

• Lead and develop a high-performing global Informed Consent Form (ICF) team, ensuring high quality, compliance, and timely delivery 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. 

• Line manage and mentor ICF managers, building capability, engagement, and a culture of excellence. 

WIN 

What we expect of you 

We 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: 

• Degree educated.

• Clinical trial execution experience and 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 

THRIVE 

What you can expect of us 

As 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.  

• 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.

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 patients above 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 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.