Senior Stats Programmer (VAX)
海得拉巴, 印度 Permanent 发布于 Apr. 07, 2026 申请截止于 Apr. 22, 2026About 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
You are a passionate leader with following experience and competences who like the challenge and growing into a new environment:
Experience:
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
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Skills:
Good understanding of processes associated with clinical trials
Ability to independently create specifications
Knowledge of descriptive statistics
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
Education:
Bachelors or Masters degree in Statistics, Mathematics, Computer Science or related health sciences or equivalent experience
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Languages:
English: Highly effective communication, both oral and written
Why choose us?
From providing protection against disease at every stage of life to protecting humanity against emerging epidemics, vaccines help create and maintain healthy communities that keep life moving forward. With a clear and strong ambition to deliver a robust Vaccines portfolio, we aim to create an environment that
Brings the miracles of science to life alongside a supportive, future-focused team
Provides opportunities for people to learn, gain experience and share knowledge
Is obsessed by leveraging your expertise in bringing data to life at the heart of decision making
Values team work and collaboration, taking care of each other, rowing all in the same direction to the finish line
Nurtures diversity and inclusion, complementing each others
Seeks constantly opportunities to re-invent ourselves
This role is critical to our team’s success and offers exposure to a broad range of activities within Biostatistics and Programming and a broad range of stakeholders.
追寻 发展。探索 菲凡。
进步需要我们每个人的参与——不论其背景、地域、或职业,我们都有一个共同的愿望:创造奇迹。你也可以成为其中的一员。我们不断追求变革,拥抱新思想,探索我们所能提供的一切机会。让我们一起追求进步。共同发现非凡。
在赛诺菲,不分种族、肤色、血统、宗教、性别、国籍、性取向、年龄、公民身份、婚姻状况、残疾或性别认同,我们为所有人提供平等的机会。
观看 “在赛诺菲的一天” ,并在官网 (sanofi.com) 上查看赛诺菲的多元化、公平与包容倡议!
共享中心
从波哥大到布达佩斯,从吉隆坡到海得拉巴,我们的版图上处处都有您的全力付出。如果您选择在共享中心施展抱负,您将身处全球变革的中心。我们无惧艰难,并肩作战,努力缩短新药抵达患者手中的时间。您将充分发挥创造力,成就独一无二的自我,从而帮助其他人拥有健康生活。让我们努力探索先进科技,改变更多人的生活。
体验可能性
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我们的故事
我们关注每一个员工的声音。因为,我们的未来取决于所有员工的付出与努力。正因为他们的助力,我们才能追求远大的理想。