Muyis Doumu is seeking a position as a Clinical Research Associate where he can utilize his qualifications in designing, researching, and closing clinical trials. He has a Master's degree in Health Administration and over 10 years of experience monitoring clinical trials and ensuring compliance with regulations. His skills include traveling up to 50% of the time, experience with medical devices and clinical trial management systems, and strong communication and problem-solving abilities. His previous roles involved monitoring multiple trial sites, recruiting and screening candidates, and drafting reports on trial progress.

1. MUYIS DOUNMU
Willingboro,NJ08046 ♦ (609) 968-9968 ♦ muyisd2@yahoo.com
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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.