#R-201426
rence materials.
As an experienced biostatistician you will establish analysis and reporting processes and good practice related to HTA, collaborating with cross-functional stakeholders.
You will provide statistical input and subject matter expertise on innovative and fit for purpose clinical trial design and data analysis to meet HTA needs.
KEY RESPONSIBILITIES
Advocate for increased knowledge within CfDA on new EU HTA regulation, its impact and implementation phases
Ensure an effective collaboration between CfDA and HEOR throughout the product lifecycle and implement strategies to increase HTA knowledge and expertise within CfDA
Provide consulting and hands-on support for CfDA team members undertaking analyses for HTA purposes
Provide statistical expertise in causal inference, indirect comparison, PRO evaluation and subgroup analysis
Development and maintenance of a range of resources for HTA purposes, including TFL shell and code library
Interact with multifunctional internal stakeholders and Subject Matter Experts to deliver value by developing novel, practical, scientific data-driven solutions to meet HTA business needs
Network with HTA Subject Matter Experts across industry
Involvement in process development and maintenance of statistical activities related to HTA
Join our team:
You would be joining a global team of statisticians, data scientists and statistical programmers in the CfDA function. The role is within the Design & Innovation subfunction, where you would engage with other team members working on innovative and cutting-edge solutions to support product teams as they work to bring transformative medicines to patients.
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 in Statistics/Biostatistics or related subject with high statistical content, coupled with post graduate statistical experience gained within biopharmaceutical industry or medical research
Superior understanding of statistical principles, methods, applications and procedures, specifically related to the HTA setting
Highly proficient in biostatistical software, including R and SAS
Life cycle drug development experience
Excellent analytical and problem-solving skills
Experience working effectively in a globally dispersed team and with cross functional partners
Excellent communication skills both oral and written
Experience in developing policies and SOPs
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.
Clear and disciplined strategic vision for the future that leverages superior-quality products, operational excellence, and top-shelf-talent
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. Fully remote working may be considered
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, colour, 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.
.