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: Performing simple design and analysis, and uses appropriate statistical software (under supervision) Identifing and begining to interpret problems in processes/results and communicates them to supervisor/manager Executing assigned tasks with high quality, integrity and attention to detail Performing Quality Control (QC) of own work Keeping manager/supervisor informed of progress and activities; escalates issues as appropriate Presenting concise summaries of own activities in group settings Preparing brief oral or written summaries of assigned work with interpretation Working effectively and collaboratively within own teamYou are: MSc. in statistics or equivalent 1+ year of experience as a statistician within the pharmaceutical area or equivalent knowledge through relevant experience Good understanding of basic trial designs and classical inference methodologies Working knowledge of Good Practice (GxP), International Council for Harmonisation (ICH) requirements Previous work experience with CDISC and SDTM / ADAM Previous work experience with SAS or R programming Previous work experience with randomization and study designPlease use the below link for job application and quicker response,https://lifelancer.com/jobs/view/3cda54dd8ff3adfd833b3b322ef9343a