Biostatistician II

Production and/or QC of derived datasets and both simple and advanced statistical outputs using efficient programming techniquesUnderstand and apply moderately advanced statistical methodsCoordinate and lead a project team to successful completion of a project within given timelines and budgetInteract with clients as key contact with regard to statistical and contractual issues Assist in the production of analysis plans, statistical reports, statistical sections of integrated clinical reports and other process supporting documentsCheck own work in an ongoing manner to ensure first-time qualityProvide training in statistical analysis to internal clientsProactively participate in and/or lead process/quality improvement initiativesTravel to, attend and actively contribute to all kind of client meetings as appropriate (eg discussing analysis concepts, presenting and discussing study resultsMentor and train junior members of the departmentAdditional responsibilities as defined by supervisor/managerSupport of Business Development, eg by attending and preparing bid defense meetingsQualificationsSkills:

Good analytical skills Good project management skills Professional attitude Attention to detail A good understanding of statistical issues in clinical trials Prior experience with SAS programming desirable Ability to work independently Good mentoring/leadership skills. Knowledge and Experience :

PhD in Statistics or related discipline entry level, MS in Statistics or related discipline with some experience The knowledge of pharmacokinetic data is an advantage Competent in written and oral English in addition to local language