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1、XXXXXDOB:MMM.YYYYGender:MaleNativeplace:XXXXXcity,XXXXXProvinceMajor:ClinicalMedicine&MolecularOncologyPhone:139XXXXXXXXEmail:XXXXXXXXObjectiveSeniorCRAorCRAII(locatedinShanghai)SummaryCertifiedCRAofACRP,March2011~May31,2013;MorethantwoyearsexperiencesasaClinicalR
2、esearchAssociate;In-depthknowledgeofHelsinkiDeclaration,ICH-GCPGuidelinesandSOPs;Self-studyofFDACFRonline;Therapeuticareasincludecancer,endocrineandcardiovasculardiseases;Goodunderstandingofmedicalterminology;FamiliaritywithEDC,IVRS/IWRSandcentrallaboratory
3、 procedures;Excellentinterpersonalskillsandfastprioritizationoftasks;Strongsenseofself-discipline;Goodspiritofteamwork;FluentinAmericanEnglishand
4、Mandarin;Enjoytravelling.Education2005~2008,Master;BiomedicalresearchesonMolecularOncology;FudanUniversity,Shanghai,China2000~2005,Bachelor;ClinicalMedicine;UniversityofSouthChinaWorkExperienceI.Mar/2011-June/2011,ResearchAssistantatBuckInstituteforResearchonAging
5、JobDescription:Assistinthedesign,preparation,implementationofexperiments,andanalysisoftheresultstoexplorethecompoundsthatcanextendlifespanofanimalmodelsandtheircorrespondingmolecularmechanisms,aswellastofindnewstrategiesforthetreatmentofneurondegenerativediseasess
6、uchasAlzheimer’sdiseaseandParkinson’sdisease;AcquiredawellunderstandingofAmericancultureandimprovedcommunicationskillsinEnglishthroughthisjob.II.Sep/2010-Mar/2011,MemberofAssociationofClinicalResearchProfessional(ACRP)(1)SystematicallylearningofICH-E6,ICH-E8,ICH-E
7、2AandACRPrecommendeddocuments,suchasGuidetoClinicalTrials;(2)PassedtheexaminationofCertifiedClinicalResearchAssociate(CCRA);(3)StudytheclinicaltrialregulationsofFoodandDrugAdministration(FDA);Page3of3(4)Involvedinthediscussionofmonitoringandmanagementofclinicaltri
8、alsinthee-ForumofACRP,builttheknowledgeonthestatusquoofclinicaltrialindustryinUS.III.Apr/2009-Aug/2010,ContractCRAinOmnicareClinicalResearch(China),base
