Page1of3
XXXXX
DOB::Male
Nativeplace:XXXXXcity,XXXXXProvince
Major:ClinicalMedicine&MolecularOncologctappropriatesitestoconductclinicaltrials;
Negotiatewithprincipalinvestigatorstoconcludeclinicaltrialcontracts;
PrepareIRB/IECsubmissiondocuments;
Conductinitiationmeetingtostartatrialwithinrequiredtimeline;
Performperiodicmonitoringvisitstodiscussrecruitmentwithinvestigators,to
verifytrialdataagainstsourcedocuments,tocoordinatewiththeresolutionofqueries,tofacilitatethereportofSAE,tocheckrecordsregardinginvestigationalproducts,toassistwiththearrangementofessentialdocuments,andultimately,toprotectthesafety,rightsandwell-beingofsubjectsandtokeephighqualityaswellasgoodprogressofclinicaltrials;
MakecloseoutvisitsaccordingtoSOP,ICH-GCPandapplicableregulations;
Liaisonbetweensiteandsponsorforotherlogisticaffairs;
WriterelevantreportsaccordingtoSOP.
Achievements:
Responsibleformonitoring2trials,including7sitesand71ongoingsubjectssimultaneously;thiswasthehighestworkloadamongallCRAsinBoehringer-,therecruitmentwasfasterthanmostcolleagues
sites,RDCverificationratewaskeptnear80%,andalltrialrelateddocumentswerefiledwellinsites;
4subjectswererecruitedwithinonemonthafterinitiationvisitofaglobalphase
;
43eligiblesubjectswereenrolledwithintwomont
临床监查员CRA求职英文简历模版 来自淘豆网www.taodocs.com转载请标明出处.