Biostatistics Sr Mgr

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📍 United States
📅 Posted 2026-07-13 · via Himalayas
🏷 Biostatistics,Clinical-Development,Statistical-Analysis,Clinical-Research,Biostatistics-Manager,Senior-Manager-Of-Biostatistics,Senior-Manager-Biostatistician,Senior-Biostatistician,Senior-Biostatistics
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Job Title: Biostatistics Sr Mgr

Job Location: Washington D.C., District of Columbia, United States

Job Location Type: Remote

Job Contract Type: Full time
Job Seniority Level:
Biostatistics Sr. Manager
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.
Biostatistics Sr. Manager
What you will do
Let’s do this. Let’s change the world.

As a Biostatistics Sr. Manager, you will lead study-level statistical deliverables with substantial independence. This role manages small teams, mentors staff and ensures the delivery of high-quality statistical outputs that meet CfDA and regulatory expectations.
Responsibilities:

- Utilizing knowledge and expertise to inform and provide sound statistical guidance to areas and teams in clinical development, reimbursement, and medical affairs.​

- Plan and execute statistical contributions to protocols, Flash Memos and Clinical Study Reports (CSRs)​

- Implement, manage and support standards, technical quality and consistent approaches in strategy, study design and statistical analysis.​

- Knowledgeable of developments in the field of statistics in drug development (innovative trial design) and Amgen’s statistical policies, procedures and strategies.​

- Understand, promote, and communicate innovative and standard statistical methodologies, trial design, data analysis, and medical / clinical understanding for product​

- Oversee statistical contributions to key design elements, protocols, randomization specifications, statistical analysis plans, tables, figures and listing shells, submission data file specifications, and other key study-related documentation​

- Collaborate cross-functionally to deliver robust, valid and scientifically rigorous analysis results in Table, Figure and Listings (TFLs), Flash Memos (FM), Clinical Study Reports (CSRs), clinical publications, and other communications​

- Serve as the GBS lead on the Clinical Study Team leadership team to execute clinical trials according to the protocol, performing risk assessments and ensuring quality data collection and alignment between data collection and study objectives​

- Contribute to clinical publications, regulatory filing documents, reimbursement documents and other communications for product or study​

- Provide statistical consultancy, training, and advice within Amgen ​

- Contributing to process improvement initiatives and operational efficiencies.​

- Oversee FSP statisticians and check their contributions for quality ​

- Ensure statistics sections of the TMF are maintained and up-to-date​

- Opportunity to manage staff, e.g. external contractors​

- Opportunity to serve as a product regional lead ​

Win

What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a strategic Biostatistics leader with a passion for tech-enabled transformation.

Basic Qualifications:

- Doctorate degree in Statistics/Biostatistics or related subject with high statistical content and

- At least 2 years of post-graduate statistical experience in the pharmaceutical industry or medical research

Or

- Master’s degree in Statistics/Biostatistics or related subject with high statistical content and

- At least 6 years of post-graduate statistical experience in the pharmaceutical industry or medical research

Or

- Bachelor’s degree in Statistics/Biostatistics or related subject with high statistical content and

- At least 8 years of post-graduate statistical experience in the pharmaceutical industry or medical research

Preferr

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