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Current Experience

  • Senior Clinical Research Associate (CRA)

    Since March 2012

Past Experience

  • Country Manager

    October 2008 --- February 2012

  • Assistant Research Officer

    September 2003 --- September 2008


Self Assessment :
Analytical thinkingAdaptabilityApproachabilityAssertivenessAttention to detailCollaborationCommunicativeCoordinationCritical thinkingDependabilityDiligenceCreative thinkingEfficiencyFlexibilityIndependenceProactivityProblem solvingResiliencyResult OrientedSelf-disciplineTrust


Self Assessment :
Biochemistry Diabetes R&D21 CFR Part 11Adverse Events (AE)Biomedical SciencesCardiovascular diseasesClinical monitoringClinical operationsClinical researchClinical trial managementClinical Trial Management System (CTMS)Clinical trialsCommunication SkillsCompliance with regulationsCustomer ServiceDNA extractionDNA sequencingDrug AccountabilityEfficacy trialsElectronic Data Capture (EDC) ElectrophoresisELISAEnglishEnzyme AssaysEnzyme-linked immunosorbent assay (ELISA)Good Clinical Practice (GCP)Good Laboratory Practice (GLP)In vitro diagnostics (IVD)INDInfectious diseasesInformed Consent DocumentsLaboratory ManagementManaging Clinical Trial SuppliesMonitoring Study ProgressPhases of clinical development (phase I to IV)Problem SolvingQA complianceSerious Adverse Event (SAE)Standard Operating Procedure (SOP)Supervising CRAsTeam LeadershipUnderstanding of regulatory guidelinesVaccines
LinkedIn Assessment :
Microsoft OfficeHealthcareClinical monitoring

Skills and Expertise

Self Assessment :
Analytical skills Build and manage the Trial Master File (TMF) Interact with physicians Interact with nurses Monitor a clinical study Report dataAssist with site trainingAttend investigator meetingAssemble regulatory applicationsAssess site feasibilityBuild trial master file (TMF)Capture data on source documentsClinical data collectionCoach and provide guidance to clinical staff.Coach clinical staffCollaborate with principal investigatorCollaborate with project teamCollaborate with PI and institution to respond to any audit findings and implement-approved recommendations.Communicate with investigatorCommunicate with sponsorSupervise clinical monitorsFacilitate sponsor monitoring visitsSchedule sponsor monitoring visitsReview monitoring reportsMonitoring enrolmentMonitor Key Performance Indicators (KPI's)Monitor dataLead teamsVerify dataTrain on site staffSerious Adverse Event (SAE) ReconciliationSchedule trial visitsReview informed consent processReview exclusion criteriaReview inclusion criteriaRespond to audit findingsRegulatory submissionsRegulatory documentationProvide trainingPrepare external auditsPre-study procedures Manage trial master file (TMF)


  • MSc in Infectious Diseases from London School of Hygiene and Tropical Diseases in 2010
  • Post Graduate Diploma in Infectious Diseases from London School of Hygiene and Tropical Diseases in 2008
  • BSc (Hons) in Biochemistry from Kwame Nkrumah University of Science and Technology in 2002

Training and Certification

  • GCP in 2015 Certification


BrightOwl Assessment:
Self Assessment:
Full Proficiency
Professional Proficiency

Work Preferences

  • Notice Period:
    4 weeks
  • Positions I am interested in:
    Senior Clinical Research Associate (CRA)
  • Locations I am interested in:
    Benin Burkina Faso Côte d'Ivoire Gambia Ghana Liberia Nigeria Sierra Leone Togo United Kingdom United States
  • Work From Home:
    Yes, 3 to 5 days per week
  • Work Regime:
    Permanent position :    100% FTE
    BrightOwl freelancer :    40 Hours per week :    100 Free Per Month(in coming months)
  • International:

Area / Region

Accra, Greater Accra, Ghana


Driving License
  • Yes

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