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:
* Responsible forplanning managing and execution of statistical deliverables inclinical trial and nontrial activities in the project
* Responsible for providing statistical input to authorityrequired documents or meetings
* Responsible forensuring that clinical trial and nontrial tasks are aligned withthe project specifications
* Deliver resultsthrough and ensure understanding among colleagues relevant forproblemsolving
* Lead project teams to achievemilestones and objectives
* Prioritize planmanage and execute Clinical Trials and submissions within projectarea
* Mentor and develop successors withinproject area
* Fully responsible for statisticalmethodology and deliverables within the project
* Main contact to stakeholders regarding statistics withinthe project
Youare:
* MSc. instatistics or equivalent
* 3 years of experienceas a statistician within the pharmaceutical area or equivalentknowledge through relevant experience
* Experience with a broad range of statisticaltasks
* Indepth knowledge of biostatisticalmethods
* Extensive experience with practicalapplications of biostatistical methodology
* Indepth knowledge of drug development
* Broad experience with statistical software and IT andindepth experience with at least one statistical softwarepackage
* Good knowledge of GCP and statisticalguidelines within drug development
* Regularexperience with communication of statistical issues andpresentations
* Basic understanding of thepharmaceutical industry and key elements of the value chain with afocus on immediate stakeholders and how to deliver on owngoals
Please use the below link forjob application and quickerresponse.
RemoteWork :
No