Biostatistics Sr Associate – Data Visualization
About this opportunity
Career Category
Clinical Development
Job Description
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 Associate
What you will do
Let’s do this. Let’s change the world.
Amgen is expanding its global Biostatistics capabilities, with Amgen India playing a key role in integrated delivery and functional leadership. As a Biostatistics Senior Associate, you will provide hands-on statistical expertise to clinical studies across the drug development lifecycle. You will author and review statistical documents, perform data analyses, and collaborate cross-functionally to ensure scientific rigor, regulatory compliance, and timely delivery of study outputs.
This role provides an opportunity to gain breadth across statistical deliverables while developing depth in clinical trial methodology, programming, and cross-functional teamwork.
Responsibilities:
Apply biostatistical methods to analyze and interpret clinical trial data
Develop and maintain statistical programming solutions using R for data analysis, reporting, and automation
Collaborate with cross-functional teams to ensure timely delivery of study outputs
Support study teams with regulatory submission deliverables following industry standards such as CDISC (SDTM, ADaM) where applicable
Stay abreast of new methodologies, tools, and regulatory guidelines in statistical practice
Build automated workflows and reproducible reporting pipelines to improve efficiency and quality of statistical outputs
Contribute to process improvements and innovative technologies that optimize statistical programming and reporting workflows
Ensure compliance with regulatory requirements and internal quality standards
Assist in reviewing Amgen policies, SOPs, and controlled documents to ensure compliance
This position is currently located at Amgen India (Hyderabad).
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 :
Master’s degree in Statistics/Biostatistics (or related subject with high statistical content) with 4 years post-graduate experience as a statistician in the pharmaceutical industry or medical research, OR
Doctoral degree in Statistics/Biostatistics (or related subject with high statistical content) with 2 year post-graduate experience.
Competency in statistical programming (R/Python).
Experience with R Shiny or interactive reporting tools
Experience applying statistical methods in the analysis and conduct of clinical trials.
Ability to clearly communicate in English, both written and oral.
Preferred Skills :
Master’s degree with 6+ years post-graduate experience, or Doctorate with 4+ years.
Prior leadership of at least 1 study/project with minimal oversight.
Experience authoring protocols, SAPs, and reviewing CSRs.
Familiarity with CDISC standards (SDTM, ADaM).
Experience with AI/automation tools to drive efficiency.
Strong understanding of drug development and statistical applications across the clinical lifecycle.
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.
Vast opportunities to learn and develop within 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
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Job details
How this role compares
Computed from every other active Clinical Development role in our database, not just this employer's listings.
We currently track 186 comparable Senior Clinical Development roles across 34 biopharma companies.
Salary context
41 of 186 peers report a salary range (USD, annualized)
Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.
Where these roles are based
Top locations among the 186 comparable roles
+ 17 more countries
Seniority mix
186 of 186 peers have a known seniority level
Therapeutic area mix
21 of 186 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.