About therole
ICON plc is a worldleadinghealthcare intelligence and clinical research organization. Wereproud to foster an inclusive environment driving innovation andexcellence and we welcome you to join us on our mission to shapethe future of clinicaldevelopment.
What you will bedoing:
* Performingsimple design and analysis and uses appropriate statisticalsoftware (under supervision)
* Identifing andbegining to interpret problems in processes/results andcommunicates them to supervisor/manager
* Executing assigned tasks with high quality integrity andattention to detail
* Performing Quality Control(QC) of own work
* Keeping manager/supervisorinformed of progress and activities; escalates issues asappropriate
* Presenting concise summaries ofown activities in group settings
* Preparingbrief oral or written summaries of assigned work withinterpretation
* Working effectively andcollaboratively within ownteam
Youare:
* MSc. instatistics or equivalent
* 1 year of experienceas a statistician within the pharmaceutical area or equivalentknowledge through relevant experience
* Goodunderstanding of basic trial designs and classical inferencemethodologies
* Working knowledge of GoodPractice (GxP) International Council for Harmonisation (ICH)requirements
* Previous work experience withCDISC and SDTM / ADAM
* Previous work experiencewith SAS or R programming
* Previous workexperience with randomization and studydesign
Please use the below link forjob application and quickerresponse
RemoteWork :
No