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

Lifelancer (https://lifelancer.com) is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech, data science and IT domains.

Please use the below Lifelancer link for job application and quicker response.

https://lifelancer.com/jobs/view/2d32082612d082bfb38fed24f4d23b6d