About the roleICON 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 experienceExtensive experience with programming in e.g. SAS or RExperience with reporting clinical trials, including statistical data handling, analysis and reportingExperience with review and documentation of programsGood knowledge of drug development.Please use the below link for job application and quicker response.https://lifelancer.com/jobs/view/b06bd9d1ad0042aa65d29cf49b84c4cb