Senior Statistical Programmer
United Kingdom
ICON Strategic Solutions
ICON people have a mission to succeed and a passion that ensures what we do, we do well. Responsibilities: Planning, managing and execution of statistical programming deliverables in clinical trial and non-trial activities in the project Providing input to authority required documents for the trial and non-trial … Ensuring that the inspection readiness documentation is updated at all time during the trial life cycle Required skills and experience: 5+ years' experience of statistical programming in clinical research or pharma Extensive experience with programming in e.g. SAS or R Experience of leading programming activities in clinical trial Experience … with reporting clinical trials, including statistical data handling, analysis and reporting Experience with review and documentation of programs Good knowledge of drug development Experience with clinical database technologies, data models and advanced programming Experience with collaboration across professional and regional borders Regular experience with communication and presentations In-depth more »
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