Informed Consent Manager
London Borough - UK
Job Summary
Career Category
ClinicalJob Description
HOW MIGHT YOU DEFY IMAGINATION
If you feel likeyourepart of something biggeritsbecause you are. AtAmgenour shared missionto serve patientsdrives all that we do. It is key to our becoming one of the worlds leading biotechnology companies. We are global collaborators who achieve togetherresearchingmanufacturingand delivering ever-better products that reachover10 million patientsworldwide.Itstime for a career you can be proud of. Join us.
INFORMED CONSENTMANAGER
LIVE
What youwill 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 expectofyou
We are all different yet we all use our unique contributions to serve patients.What weseekin you as anexperiencedprofessional 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 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.
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.
Required Experience:
Manager
Key Skills
About Company
Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses. As an organization dedicated to improving the ... View more