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    Job · 15442992

    Sanofi logo

    Principal Stats Programmer (VAX)

    Sanofi · Hyderabad · onsite · Posted 48d ago

    Undisclosed8–12 yrsfulltimeSourced fromNaukri

    About a minute. You'll make an account on the way through.

    About this role

    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 Principal 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:

    • Plan and execute high quality and timely statistical programming deliverables in the context of a vaccine project
    • At study level for various analyses within a study:
    • Review and provide feedback on study documents (e.g.: protocol statistical section, Case Report Form, Statistical Analysis Plan (SAP)); create 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
    • At project level for various analyses within an asset:
    • Review and provide feedback on integrated analysis plan and create mock TLFs
    • Create core integrated clinical database, pooling SDTM/ADaM across several studies for different reporting purposes like ISS/ISE/ISI, DSUR, PBRER or safety surveillance
    • Ensure TLF's format fulfil the requirements of targeted publishing (i.e.: clinical study report, publication, Transparency like Eudract, CTT.gov, lay summaries,...)
    • Take leadership, guiding more junior staff and ensuring quality and timely deliveries
    • Perform quality control for statistical programming deliverables and complete the associated documentation: Validation plan and quality control (QC) documentation.
    • Propose and Program exploratory and/or post hoc analyses based on problem statement
    • 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:

    • 8+ 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 in providing solutions for complex programming issues (including creation of complex macros), presenting alternatives and identifying the best solution
    • Experience pooling data from multiple studies according to existing specifications
    • Experience planning and drafting specifications for pooling data from multiple studies
    • Consistent successful experience as a lead on several concurrent studies/projects
    • e-submission preparation experience strongly preferred


    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
    • Ability to lead complex and large tasks, demonstration of strong project management skills


    Education:

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


    Languages:

    • English: Highly effective communication, both oral and written

    Sourced from naukri

    Skills

    SAPPbreradamclinical researchclinical trialsmathematicsStatistical programmingProgrammingSdtmProgrammermetadataCdiscSASclinical study reportconcurrentHealthcareSQLProject ManagementQuality ControlResearchcomplianceQC

    About Sanofi

    Sanofi logo

    Sanofi

    Pharma

    3k+

    employees

    1956

    70 years old

    Mumbai, Maharashtra

    India

    About

    Sanofi provides potentially life-changing treatments and the protection of life-saving vaccines to millions of people

    Industries

    PharmaBiotech & Life sciencesManufacturingAnalytics & KPO

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