Statistical Programmer
Found in: Whatjobs IN C2 - 2 weeks ago
About the role
ICON plc is a world-leading healthcare intelligence and clinical research organization. Were proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
What you will be doing:
Responsible for planning, managing and execution of statistical programming deliverables in clinical trial and non-trial activities in the project
Responsible for providing input to authority required documents for the trial and non-trial activities
Responsible for ensuring that clinical trial and non-trial tasks are aligned with the project specifications
Responsible for continuous development of own skills and to contribute to the development of Biostatistics
You are:
- +3 years of statistical programming, and preferably 1 year within the pharmaceutical industry or equivalent knowledge through relevant experience
- Extensive experience with programming in e.g. SAS or R
- Experience with reporting clinical trials, including statistical data handling, analysis and reporting
- Experience with review and documentation of programs
- Good knowledge of drug development
Please use the below link for job application and quicker response.
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