Training

Chair: Gemma Hodgson

The PSI Training Committee organises five or six training courses each year. Generally our courses are designed to bring statisticians and statistical programmers working in the pharmaceutical industry up-to-date in a particular subject area. Courses are of one or two days' duration, and our presenters are often from academia with particular expertise in the course topic. We focus on application, but also provide sufficient theory to clarify the concepts behind the techniques. Delegate numbers are limited to 30 or less so that there is plenty of opportunity for questions and discussion.

In addition we work with other professional groups and run an annual training course for statisticians new to the industry.  


For further details or to register for future training courses please click here 

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EventsFuture Events


  • Expert Working Group on Confidentiality of Interim Results - Dates: 11 May, 2017

    The PSI/EFSPI expert working group on Confidentiality of Interim Results are planning to meet face to face on 11 May.
  • Estimating Sample Sizes in Clinical Trials - Dates: 28 – 29 Jun, 2017

    The three most important aspects of a clinical trial are: design, design and design. A sample size estimate is just one aspect of a clinical study design. The course describes calculations for sample size estimation in the design of clinical trials. It will be highlighted how the objectives of a clinical trial will impact on sample size calculations. The course is a practical course and all methods will be illustrated with examples and case studies.
Leeds-80x250

Medical Statistician / Senior Medical Statistician

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Director, Statistics

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Astrazeneca

Associate Director, Statistics Team leader - Early Clinical Development

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Astrazeneca

Early Clinical Development – various levels

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Biostatistics Head of Department

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Astrazeneca

Principal Statistician – Centralised Statistical Monitoring

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Astrazeneca

Clinical Trial Design Methodology Expert - Statistical Innovation Team

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