Amgen Technology Pvt Ltd. Posted September 29, 2026

Biostatistical Programming Senior Associate (Innovation)

Hyderabad, India Full time
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Amgen Technology Pvt Ltd. is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Career Category

Clinical

Job Description

Biostatistical Programming Senior Associate ( Innovation)

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.

 

Biostatistical Programming Senior Associate (Innovation)

NOTE: THIS ROLE DIFFERS FROM A TRADITIONAL STATISTICAL PROGRAMMING POSITION.

What you will do

Let’s do this. Let’s change the world.

Amgen is expanding its global Statistical Programming capabilities, with Amgen India (AIN) playing a key role in supporting integrated delivery across regions. As a Biostatistical Programming Senior Associate, you will focus on developing programming efficiencies, automation solutions, and innovative tools that enhance productivity and scalability across programming teams. This position is ideal for candidates who enjoy building systems and optimizing workflows, not for those primarily seeking to perform hands on statistical programming activities to support complex statistical data analysis of clinical studies and regulatory submissions.

Key Responsibilities:

Analysis and reporting of clinical trial data using SAS and/or R or Python

Creation and validation of complex SDTM, ADaM, and other analysis datasets, both safety and efficacy

Creation and validation of complex tables, listings, and figures, both safety and efficacy

Prepare statistical programming specifications

Prepare statistical programming related documents for regulatory submissions

Maintain tracking and validation documentation

Collaborate with cross-functional team and create and/or validate complex programs for checking data quality

Interact and collaborate with study team members from other functions globally

Assist in some of the tasks of the Study Lead Programmer (SLP) or serve as a backup SLP

Design, build, and maintain programming solutions and tools that improve efficiency and quality across statistical programming ecosystems.

Contribute to the full development lifecycle, from requirements gathering and design through testing, deployment, and maintenance.

Collaborate with programming teams across center for design and analysis (CfDA) to identify process gaps and prototype scalable solutions using modern programming practices.

Support federated innovation, integrating ideas and code contributions from other programming teams into unified, CfDA-wide solutions.

Automate repeatable programming tasks and establish standards for modular, reusable code.

Leverage AI and machine learning capabilities, including developing and deploying AI agents or copilots, to optimize programming workflows and knowledge sharing.

Create and maintain clear, version-controlled documentation, training materials, and user guides to enable sustainable adoption of new tools.

Participate in ongoing evaluation and enhancement of tools, ensuring continued performance, security, and relevance.

Collaborate with cross-functional partners to align innovations with business needs and technical standards.

This position will be 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 results-oriented, tech-forward programming leader with deep expertise in clinical trial operations and digital transformation.

Basic Qualifications :

Bachelor’s or higher degree in biostatistics, statistics, mathematics, AI and data science, computer science, or other related quantitative or scientific subjects, with at least 4 years of statistical programming experience in relevant career statistical programming experience in a clinical development environment.

Familiarity with drug development life cycle and excellent skills with the manipulation, analysis and reporting of complex clinical trial data

Ability to effectively perform complex statistical programming and related tasks

Ability to provide quality output and deliverables in adherence with challenging timelines

Ability to work effectively on multiple tasks or projects across therapeutic areas

Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners

Working knowledge of latest CDISC SDTM standards and familiar with CDISC ADaM and Define standards with strong ability to implement the standards

Familiar with data quality and compliance check tools

Excellent oral and written English communication skills

Preferred Skills :

Masters or higher degree in statistics, biostatistics, mathematics, AI and data science, computer science or related quantitative or scientific subjects

Familiarity with open-source programming tools (R, Python), automation platforms, and emerging technologies in statistical programming

Experience developing or maintaining solutions through a structured software development lifecycle (SDLC).

Experience:

SAS macro development

R/Python Package development

Working knowledge of version control (e.g., Git) and collaborative coding practices.

Familiarity with AI and machine learning frameworks (e.g., OpenAI API, or custom model training).

Building or implementing AI-driven programming assistants, copilots, or agents for workflow optimization.

Working knowledge of Agile project management and collaborative development environments.

Competencies:

Strong programming (e.g., SAS, R, SQL, Python) and analytic skills

Innovation and problem solving

Strong documentation and communication skills

Collaboration and teamwork across functions

Organization and follow-through in structured projects

AI and automation mindset

Learning agility and curiosity

 

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 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

.

Job details

Seniority
Senior
Function
Clinical Development
Therapeutic area
Not listed
Location
Hyderabad, India
Employment type
Full time

How this role compares

Computed from every other active Clinical Development role in our database, not just this employer's listings.

We currently track 227 comparable Senior Clinical Development roles across 52 biopharma companies.

227Comparable roles tracked
217Currently active
52Companies hiring similar roles
20Countries represented

Salary context

82 of 227 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.

This roleSubject Not listed on this posting
Lowest disclosed · Senior Administrative Assistant - Clinical Development Operations · AbbVie $27/hr – $48/hr (≈ $56,160–$99,840/yr)
Peer group range $78,000 – $363,200 (median $199,500)

Where these roles are based

Top locations among the 227 comparable roles

United States110
India44
United Kingdom14
Taiwan10
Spain8
Poland7

+ 14 more countries

Seniority mix

227 of 227 peers have a known seniority level

Associate Director102
Senior101
Principal24

Therapeutic area mix

28 of 227 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology18
Neuroscience5
Immunology3
Dermatology & Aesthetics1
Ophthalmology1

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.

60%similar
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60%similar
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60%similar
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60%similar
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Same function Same seniority Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

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.

60%
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Function Therapeutic area Seniority Country
60%
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Study Delivery Sr Associate
Amgen Technology Pvt Ltd. · Hyderabad, India · Senior
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60%
Biostatistical Programming Senior Associate
Amgen Technology Pvt Ltd. · Hyderabad, India · Senior
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 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.