Senior Statistical Programmer

About the role
As a Senior Statistical Programmer I you will be joining the worlds largest most comprehensive clinical research organisation, powered by healthcare intelligence.
What you will be doing:

• Provide programming input to the design of the trial
• Provide input to the blinding of the clinical trial
• Ensure ADaM programming is done according to industry standard and NN specifications
• Ensure that programming, also by co-workers and functional suppliers, is done according to specifications
• Ensure that the inspection readiness documentation is updated at all time during the trial life cycle
• Ensure good contact and collaboration with Data Management and Clinical Data Standards

You are:

• 5+ years in the biological area doing statistical programming and system development, and of these preferably 3 years within the pharmaceutical industry
• Extensive experience with programming in e.g. SAS or R
• Extensive experience with reporting clinical trials, including statistical data handling, analysis and reporting.
• Extensive experience with review and documentation of programs
• In depth knowledge of drug development

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