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muyis Dosunmu
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MUYIS DOUNMU Willingboro,NJ08046 ♦ (609) 968-9968 ♦ muyisd2@yahoo.com ____________________________________________________________________________________ OBJECTIVE Seekingforthe positionof aClinical ResearchAssociate inthe medicalfieldthatwill utilize my qualificationswhile offeringseveral opportunitiestoapplymydesigning,researchingandclosingclinical trialsskills. EDUCATION Master of HealthAdministration(MPA) –May 2007 - KeanUniversity,Union,NJ BA Sociology/Collateral- AfricanaStudies - May2005 - KeanUniversity,Union,NJ Certifications: NJState Licenses - NJCertifiedNursingAssistant-CNA,NJCPR,NJCPI,NJMedication. Phlebotomist,Clinical ResearchCoordinator- 2008 Summaryof Skills: •Ability/willingnesstotravel upto 50% •Experience withMedical device experience andProficientinMSOffice Suite of products •Experience withClinical Trial ManagementSystem •Experience withEDCsystemandexcellentinterpersonal andcommunicationskills •Provenabilitytodemonstrate strongdecisionmakingandproblemsolvingskills Experience: Clinical ResearchAssociate Virtual,LumbertonNJ 2011 - Present •Monitor multiple clinicaltrial sitesandstudies. •Recruitingandscreeningcandidatesforclinical trials •Responsibleforsite monitoring,sitemanagement,siteadministrationandregistrymanagementfor clinical studiesaccordingtoGCP,ICH andFDA guidelines,andCovance StandardOperatingProcedures •Actingas a leadCRA or local projectcoordinatorinassignedprojects •Coordinatingstaff activitiesandsupervisingjuniorstaff •Ensuringfollowingof properprotocol byvisitingtestingsites
•Draftingand maintainingreportsonfindingsandprogressof trials Clinical ResearchAssociate HealthINC,SouthBrunswick,NJ 2008 - 2011 •Monitoredthe clinical trial progress •Documentthe progressof trialsand deliveredthe reportstothe management •Assistedinthe designing,implementation,choosingparticipants,andschedulingtrials •Coordinatedwithinvestigatorsandsite workers •Monitoredhumanreactionstonewdrugs andpreparedreportfor furtherchanges •Responsibleforsite training,regulatorydocumentcollection,trackingenrollment,andensuringcase reportformsare accurate, complete andverifiable againstsource documents. •Monitor multiple clinicaltrial sitesandstudies. •Contribute tothe developmentandimprovementof companyprocedures,processes,andtemplatesin supportof company’seffortstowardscontinuousqualityimprovement. Reference: Onrequest.

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Resume cra N2

  • 1. MUYIS DOUNMU Willingboro,NJ08046 ♦ (609) 968-9968 ♦ muyisd2@yahoo.com ____________________________________________________________________________________ OBJECTIVE Seekingforthe positionof aClinical ResearchAssociate inthe medicalfieldthatwill utilize my qualificationswhile offeringseveral opportunitiestoapplymydesigning,researchingandclosingclinical trialsskills. EDUCATION Master of HealthAdministration(MPA) –May 2007 - KeanUniversity,Union,NJ BA Sociology/Collateral- AfricanaStudies - May2005 - KeanUniversity,Union,NJ Certifications: NJState Licenses - NJCertifiedNursingAssistant-CNA,NJCPR,NJCPI,NJMedication. Phlebotomist,Clinical ResearchCoordinator- 2008 Summaryof Skills: •Ability/willingnesstotravel upto 50% •Experience withMedical device experience andProficientinMSOffice Suite of products •Experience withClinical Trial ManagementSystem •Experience withEDCsystemandexcellentinterpersonal andcommunicationskills •Provenabilitytodemonstrate strongdecisionmakingandproblemsolvingskills Experience: Clinical ResearchAssociate Virtual,LumbertonNJ 2011 - Present •Monitor multiple clinicaltrial sitesandstudies. •Recruitingandscreeningcandidatesforclinical trials •Responsibleforsite monitoring,sitemanagement,siteadministrationandregistrymanagementfor clinical studiesaccordingtoGCP,ICH andFDA guidelines,andCovance StandardOperatingProcedures •Actingas a leadCRA or local projectcoordinatorinassignedprojects •Coordinatingstaff activitiesandsupervisingjuniorstaff •Ensuringfollowingof properprotocol byvisitingtestingsites
  • 2. •Draftingand maintainingreportsonfindingsandprogressof trials Clinical ResearchAssociate HealthINC,SouthBrunswick,NJ 2008 - 2011 •Monitoredthe clinical trial progress •Documentthe progressof trialsand deliveredthe reportstothe management •Assistedinthe designing,implementation,choosingparticipants,andschedulingtrials •Coordinatedwithinvestigatorsandsite workers •Monitoredhumanreactionstonewdrugs andpreparedreportfor furtherchanges •Responsibleforsite training,regulatorydocumentcollection,trackingenrollment,andensuringcase reportformsare accurate, complete andverifiable againstsource documents. •Monitor multiple clinicaltrial sitesandstudies. •Contribute tothe developmentandimprovementof companyprocedures,processes,andtemplatesin supportof company’seffortstowardscontinuousqualityimprovement. Reference: Onrequest.