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i am a Clinical Research Associate/ Pharmaceutical Scientist and i have experience working as a Student Clinical Research Associate with william harvey research institute london, saint bartholomew Hospital london, royal london Hospital. etc.. i have more than four years research experience in the field of clinical research and more than two years experience in Pharmaceutical Marketing.( Medical Representative.) i am available to work in any european, african and american countries.


Past Experience

  • Clinical Research Associate/ Pharmaceutical Scientist

    April 2011 --- August 2015

  • Student Clinical Research Associate.

    December 2002 --- November 2006
    1. carrying out Research study on the effect of nitric oxide on micro circulatory blood flow in sickle Cell ss patients. 2. weighing out samples of sodium nitrate 3. carrying out urinalysis 4. carrying out measurement of micro Vascular using laser doppler flux meter. 5. carrying out measurement of rate of oxygen using trans cutaneous oxygen meter 5. carrying out measurement of rate of carbon dioxide using trans cutaneous carbon dioxide. 6. carrying out measurement of blood pressure, temperature , ecg and body weight on patients. 7. writing and reporting the Research in form of dissertation 8. Editing of project. 9. writing abstract journal and publishing journals.


Self Assessment :
Analytical thinkingAttention to detailAdaptabilityAggressivenessAuthenticityCommunicativeCharmCreative thinkingCollaborationCritical thinkingAssertivenessApproachabilityDiligenceEfficiencyCompetitivenessDominanceFlexibilityCoordinationIndependenceCuriosityInnovative thinkingInterest in knowledgeKindnessOptimismOrganizationOrientation


Self Assessment :
Biostatistics Biochemistry Medical devices Phase I R&D Scientific writingA rising single dose tolerance studyActions and modes of action of drugs in the human species NegotiationActions and modes of action of human physiologyAllergy and immunologyAnalytical techniquesAnimal Models LabtechnicianAntibodiesAutomationBioavailabilityBiochemistryBioinformaticsBiological Drug DevelopmentBiomarkersBiopharmaceuticalsBiotechnologyBudget ManagementAnesthesiaBudget ProcessCancer DiabetesCardiologyCardiovascular diseases
LinkedIn Assessment :
Clinical researchResearchMicrosoft OfficeSocial MediaPublic SpeakingCustomer ServicemanagementTeam LeadershipDrug DevelopmentLeadership

Skills and Expertise

Self Assessment :
Design case record forms Develop clinical trial protocols Create SOPs Develop protocols Interact with nurses Guide students Control data Assure medical quality Analyze data Monitor a clinical study Interpret data Receptor Pharmacology Molecular Diagnostics Interact with physicians Search literature on clinical trials Technology research Use a confocal microscopy Use content management systems Write papersAdjust processes Adjust methodsAdminister supply request Report data Lab scale batchesAdverse event reportingAdvise on medical perspectivesAnalyze dataAnalyze protein Build and manage the Trial Master File (TMF)Administrative supportApprove consent documentsApprove drug supply Approve Label Master SheetApprove monitoring reportsApprove patient informationApprove queriesArchive documentationArchive study documentsAssess adverse reactionsAssess site feasibilityAssess subject safetyAssign activitiesAssist study siteAssist with experimentsAssist with proceduresAssist with routine testsAssure medical qualityAttend investigator meetingAttend seminarsAttend steering committeeBiomarker Researchbudgeting of R&D activitiesBuild CMC development planAdjust processes and methods


  • Master of Science Degree in Clinical Drug Development. from Bart and The London Queen Mary School of Medicine and Dentistry in 2005
  • Bachelor of Science degree in Pharmaceutical sciences from University of Greenwich London in 2002

Training and Certification

  • Pharmaceutical Marketing in 2015 Training

Work Preferences

  • Notice Period:
    1 week
  • Positions I am interested in:
    Clinical Research Associate (CRA) Clinical Safety Associate Clinical Trial Administrator Clinical Trial Specialist (CTS) Clinical Trial Assistant (CTA) associate Clinical Project Manager Clinical Research Manager Clinical Trial consultant Clinical Research Associate (CRA) Freelance Science Writer Graduate Research Assistant Drug Safety Officer Medical Writer Pharmacovigilance Officer Research Scientist Senior Clinical Trial Assistant (CTA) Regulatory Affairs Associate Senior Clinical Trial Assistant Research Assistant Research associate
  • Work From Home:
  • Work Regime:
    Permanent position :    Bright Owl employee% FTE
  • International:


    Expert has 1 publications (Will be avalible with full profile)

Area / Region

Abuja, Federal Capital Territory, Nigeria


Driving License
  • Yes

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