为了让HR同事及时与您联系以便获得更快的简历反馈,请您登录精鼎医药官方网站Jobs.Parexel搜索R0000021332投递您的简历进行职位申请。职责描述:AtParexel,theCRAroleofferstheopportunitytogobeyondtheroleofatypicalclinicalmonitor.CRA’sareaccountableforusingtheirexpertisetobuildandmaintainthesiterelationshipandensurethey’resetupforsuccess.Astheclinicalsites’solepointofcontact,thisincludesaddressingandresolvingsiteissuesandquestions.You’llalsomanagesitequalityanddeliveryfromsiteidentificationthroughtoclose-out.AsaCRA,Parexelwillofferyoutechnologyandtrainingcateredtoyourindividualexperience.Youcananticipatelesstravelandalowerprotocolloadincomparisontoindustrypeers.Yourhardworkmayberewardedthroughabonusincentiveprogram,theopportunitytoworkwithinmultipletherapeuticareasandanopportunitytoadvanceyourcareerinclinicalresearch.Ifimpact,flexibility,andcareerdevelopmentappealtoyou,Parexelcouldbeyournexthome.Whatyou’lldoLeverageyourexpertise.Conductqualificationvisits(QV),siteinitiationvisits(SIV),monitoringvisits(MV)andterminationvisits(TV)atassignedclinicalsitesandgeneratevisit/contactreports.Buildrelationships.Overseeintegrityofthestudyandutilizeproblem-solvingskillstopromoterapportwiththesiteandstaff.Protectpatients.Reviewtheperformanceofthetrialatdesignatedsites,ensuretherightsandwell-beingofhumansubjectsaresafeguardedandareinaccordancewithprotocol.Driveproductivity.Developpatientrecruitmentstrategiesinconjunctionwiththeclinicalsitetomeetenrollmenttimelines,whilealsoensuringcompliancewiththeapprovedstandardoperatingprocedures(SOPs),protocol/amendment(s),GCP,andtheapplicableregulatoryrequirement(s).Ensurequality.Evaluatethequalityandintegrityofthereporteddata,siteefficacyanddrugaccountability.Execute.MonitorthecompletenessandqualityofRegulatoryDocumentationandperformsitedocumentverification.行业要求:全部行业
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