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- Tasks: Manage and deliver high-quality informed consent forms for global clinical studies.
- Company: Join Amgen, a leading biotechnology company dedicated to serving patients.
- Benefits: Flexible work options, generous rewards, and opportunities for personal growth.
- Why this job: Make a real impact in healthcare by supporting innovative medicines for patients.
- Qualifications: Degree educated with experience in clinical trials and project management.
- Other info: Be part of a diverse community that values your ideas and contributions.
The predicted salary is between 36000 - 60000 £ per year.
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.
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. 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 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.
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 experience working within a global team structure as well as project management experience
- Previous experience in life sciences or a related field, including biopharmaceutical clinical research.
- Experience in authoring ICF forms and in a clinical setting e.g. clinical site role is preferred.
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.
In our quest to serve patients above all else, Amgen is the first to imagine, and the last to doubt. Join us.
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.
Informed Consent Manager in London employer: Amgen
Contact Detail:
Amgen Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Informed Consent Manager in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, especially those who work at Amgen or similar companies. A friendly chat can open doors and give you insider info that could help you stand out.
✨Tip Number 2
Prepare for interviews by practising common questions related to informed consent management. We recommend role-playing with a friend or using online resources to get comfortable discussing your experience and how it aligns with the job.
✨Tip Number 3
Showcase your passion for patient-centric approaches! During interviews, share examples of how you've improved processes or engaged with patients in previous roles. This will highlight your commitment to the mission at Amgen.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take the initiative to connect directly with us.
We think you need these skills to ace Informed Consent Manager in London
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter for the Informed Consent Manager role. Highlight your relevant experience in clinical trials and ICF authoring, showing us how you can contribute to our mission of serving patients.
Showcase Your Team Spirit: We love collaboration! In your application, share examples of how you've worked within global teams or managed projects. This will help us see how you fit into our diverse and inclusive community.
Be Clear and Concise: When writing your application, clarity is key. Use straightforward language and avoid jargon where possible. We want to understand your qualifications and passion without any confusion!
Apply Through Our Website: Don’t forget to submit your application through our website! It’s the best way for us to receive your details and ensures you’re considered for the role. Plus, it’s super easy!
How to prepare for a job interview at Amgen
✨Know Your ICFs Inside Out
Before the interview, make sure you thoroughly understand informed consent forms (ICFs) and their role in clinical studies. Familiarise yourself with the key components of ICFs, including regulatory requirements and patient-centric language. This will help you demonstrate your expertise and show that you're ready to contribute from day one.
✨Showcase Your Collaboration Skills
Since this role involves working closely with Study Delivery Teams and Patient Engagement teams, be prepared to discuss your experience in collaborative environments. Share specific examples of how you've successfully partnered with others to achieve project goals, especially in a global context. This will highlight your ability to work effectively within diverse teams.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills and ability to handle challenges related to ICF management. Think of scenarios where you had to resolve issues quickly or implement improvements in processes. Practising these responses will help you articulate your thought process and decision-making skills during the interview.
✨Emphasise Your Commitment to Patient-Centricity
Amgen values a patient-centric approach, so be ready to discuss how you’ve incorporated patient feedback into your work. Share examples of how you’ve improved clarity and usability in ICFs or other documents. This will show that you align with their mission and are dedicated to serving patients effectively.