Senior Statistician

  • Sydney NSW, Australia
  • Full-time

Company Description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do.  A dynamic, global company founded in 1995, we bring together more than 2,000 driven, dedicated and passionate individuals.  We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

    Job Description

    Senior Statistician is an integral part of our team here at PSI. If you have experience in clinical research, understand SAS programming principles and concepts, and have a good knowledge of statistical methods, apply today! PSI Statisticians are responsible for statistical methodology and statistical analysis of assigned clinical studies.   They liaise with PSI project teams and business partners globally on statistics project-related matters.

    Office-based or Home-based

    You will:

    • Lead all biostatistics activities related to clinical trials
    • Communicate with project teams, clients and vendors on statistical questions
    • Develop and review statistical sections of protocols, including sample size calculations
    • Develop of statistical analysis plans
    • Develop and document analysis database structures (i.e. SAS analysis data set structures)
    • Develop SAS program requirements and specifications
    • Review and ensure quality control of statistical deliverables (tables, listings, figures, etc.)
    • Perform statistical analysis and report results
    • Provide consultation on experimental design, statistical methods and approaches for the purpose of assessing safety and efficacy of drug products
    • Liaise with Data Management on statistical questions, including coordination of data transfers from Data Management to Statistics
    • Participate in bid defense meetings and kick-off meetings
    • Conduct  project-specific and general training of statisticians and SAS programmers

    Qualifications

    • MSc in Statistics or equivalent
    • Experience in clinical research, biostatistics and SAS programming
    • Understanding of  statistical principles, concepts, methods, and standards used in clinical research
    •  Ability to apply a range of advanced statistical techniques, analyze, interpret, and draw conclusions from complex statistical information
    • Presentation and communication skills
    • Full working proficiency in English
    • Analytical, organizational and time management skills
    • Advanced knowledge of SAS software
    • Advanced knowledge of CDISC ADaM IG 1.0 or later, define 1-0-0.xml and define 2-0-0.xml specifications
    • Knowledge of CDISC SDTM IG 3.1.3 or later; nQuery Advisor software is a plus

    Additional Information

    Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.

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