Biostatistics Senior Manager - HTA

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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.
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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.

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