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Job Description

Key AccountabilitiesOperational ExecutionProduction 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 issuesAssist 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 resultsGeneral ActivitiesMentor and train junior members of the departmentAdditional responsibilities as defined by supervisor/managerBusiness DevelopmentSupport of Business Development, eg by attending and preparing bid defense meetingsSkillsGood analytical skillsGood project management skillsProfessional attitudeAttention to detailA good understanding of statistical issues in clinical trialsPrior experience with SAS programming desirableAbility to work independentlyGood mentoring/leadership skillsKnowledge And ExperiencePhD in Statistics or related discipline entry level, MS in Statistics or related discipline with some experienceThe knowledge of pharmacokinetic data is an advantageCompetent in written and oral English in addition to local languageEducationPhD in Statistics or related discipline, MS in Statistics or related discipline

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