Senior Stats Programmer (VAX)

Reposted Yesterday
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Hyderabad, Telangana, IND
In-Office
Senior level
Healthtech
The Role
Execute statistical programming for SDTM/ADaM and TLFs across vaccine clinical studies, draft and review specifications, deliver CDISC-compliant data packages, perform QC, pool multi-study data, and ensure SOP and regulatory compliance.
Summary Generated by Built In
Job title: Senior Statistical Programmer
  • Location: Hyderabad
About the job

Our Hubs are a crucial part of how we innovate, improving performance across every Sanofi department and providing a springboard for the amazing work we do. Build a career and you can be part of transforming our business while helping to change millions of lives.

Ready? As a Senior Statistical Programmer within our Hyderabad Hub, you’ll be part of a performing team, delivering biostatistics and programming activities throughout the Vaccines R&D value chain (Pre-Clinical, Clinical, Translational, CMC) with our Vaccines Global Biostatistical Sciences team.

We are an innovative global healthcare company that helps the world stay ahead of infectious diseases by delivering more than 500 million vaccine doses a year. Across different countries, our talented teams are exploring new technologies to protect people and promote healthy communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world.

Main responsibilities:
  • Perform programming activities for all statistical deliverables (i.e.: SDTM, ADaM, Tables Listings and Figures (TLF)) for various analyses within a study (e.g.: interim/final analyses, internal or external data monitoring committees, statistical surveillance) or within a project (i.e.: ISS, ISE, ISI, DSUR, PBRER,)

  • Review and provide feedback on study documents, such as protocol (statistical section), Case Report Form (CRF), Statistical Analysis Plan (SAP) and mock TLFs

  • Write and provide the programming specifications for the SDTM/ADaM/TLFs to fulfil the study or project objectives

  • Deliver compliant CDISC data package with all relevant documentation (ie: aCRF, reviewers guide, define.xml) fulfilling Heath Authorities expectations

  • Ensure TLF’s format fulfil the requirements of targeted publishing (i.e.: clinical study report, publication, Transparency like Eudract, CTT.gov, lay summaries,)

  • Perform quality control for statistical programming deliverables and complete the associated documentation: Validation plan and quality control (QC) documentation.

  • Program exploratory and/or post’hoc analyses with minimum specifications

  • Create core integrated clinical database, pooling SDTM/ADaM datasets across several studies within an asset

  • Ensure compliance to SOP's, standards, and guidelines.

 About you
  • 5-7 years' experience in statistical programming clinical research with some Vaccines experience (designs, endpoints, statistical methods, …)

  • SAS (>3 years): excellent technical skills in BASE, STAT, MACRO, GRAPH, SQL, R, and familiar in statistical programming

  • Experience programming CDISC SDTM/ADaM datasets and notably vaccines specifics (including writing specifications, P21, proficiency with controlled terminology, value-level metadata, analysis results metadata, define.xml, Reviewers Guide)

  • Experience pooling data from multiple studies according to existing specifications

  • Experience planning and drafting specifications for pooling data from multiple studies

  • Ability to independently create specifications

  • Knowledge of descriptive statistics

  • Good understanding of processes associated with clinical trials

  • Demonstrate interpersonal skills necessary for effective teamwork

  • Demonstrate ability to organize multiple work assignments and establish priorities

  • Demonstrate critical thinking skills beyond simply following directions or specifications

  • Bachelors or Masters degree in Statistics, Mathematics, Computer Science or related health sciences or equivalent experience

  • English: Highly effective communication, both oral and written

Pursue progress, discover extraordinary Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people. At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity. Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

Skills Required

  • 5-7 years experience in statistical programming in clinical research with vaccines experience
  • SAS (>3 years) with strong BASE, STAT, MACRO, GRAPH skills
  • Proficiency in SQL and R
  • Experience programming CDISC SDTM and ADaM datasets, writing specifications and define.xml
  • Familiarity with CDISC controlled terminology, value-level metadata, and analysis results metadata
  • Experience creating pooled/integrated clinical databases across multiple studies and drafting pooling specifications
  • Ability to independently create programming specifications
  • Knowledge of descriptive statistics and clinical trial processes
  • Strong written and oral English communication skills
  • Bachelor's or Master's degree in Statistics, Mathematics, Computer Science, or related field (or equivalent experience)
  • Ability to organize multiple assignments, prioritize work, and demonstrate critical thinking

Sanofi Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Sanofi and has not been reviewed or approved by Sanofi.

  • Retirement Support — Retirement support stands out through a notably strong 401K matching structure (e.g., 150% match up to a 6% contribution), which materially boosts total rewards for long-tenured employees.
  • Parental & Family Support — Parental and family support is positioned as unusually robust, including a global gender-neutral paid parental leave standard (14 weeks) and added supports such as childcare assistance and adoption/surrogacy/infertility help.
  • Equity Value & Accessibility — Equity participation is made more accessible via an Employee Stock Purchase Plan that includes a meaningful purchase discount and matching/free-share mechanics, increasing perceived total compensation beyond base pay.

Sanofi Insights

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The Company
HQ: Paris
85,000 Employees
Year Founded: 1973

What We Do

We are Sanofi, an innovative global healthcare company. We chase the miracles of science to improve people’s lives. Our team, across some 100 countries, is dedicated to transforming the practice of medicine by working to turn the impossible into the possible. We provide potentially life-changing treatment options and life-saving vaccine protection to millions of people globally, while putting sustainability and social responsibility at the center of our ambitions. Interactions with this account must comply with the Terms: https://bit.ly/sanofi-terms

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