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I am a Bsc (biomedical Science), currently pursuing an MSc (Epidemiology and Biostatistics) with 9 years of experience in clinical trials (Phase 2b and Phase III), cohort and crossectional studies as a laboratory manager and site/study coordinator. I am currently the National Coordinator for the Integrated Bio-Behavioural Survey for Key Populations in Kenya.

I am results driven person, able to relate professionally and prefer working in an environment that encourages team work. I have strong language and presentation skills, tech savvy and always looking to improve my skills and experience through new challenges. I have always wanted be launch a career as a CRA or CPM. This is what I am currently looking for.


Current Experience

  • Coordinator, IBBS
    Since May 2016

Past Experience

  • Study Coordinator Kisumu
    January 2014 --- December 2015

    Coordinating a two-year HIV treatment cohort aimed at observing inflammatory and coagulatory biomarkers as well as cardiovascular events

  • Lab Manager/Assistant Project Coordinator
    February 2011 --- February 2014
    Coordinating two Pfizer - funded Phase III clinical trials comparing azithromycin-chloroquine and sulfadoxine-pyrimethamine for malaria prophylaxis in pregnancy (IPTp)

  • QC/QA Officer
    July 2009 --- January 2011

     Data cleaning and auditing for various HIV clinical research and patient care centers  Source document verification  Standardization of patient flow to ensure completeness of data  Design of data capture tools  Tracing and verification of laboratory data  Reporting on audit outcomes

  • Laboratory Manager
    June 2007 --- September 2008
    Managing two MMV-funded Phase III clinical trial comparing Pyramax (pyronaridine-artesunate) and Coartem in the treatment of uncomplicated malaria in children and adults


Self Assessment :
AdaptabilityApproachabilityAttention to detailCommunicativeCoordinationEfficiencyIndependenceFlexibilityProactivityProblem solvingSociabilityStrategic thinking


LinkedIn Assessment :
molecular biologyClinical trialsLaboratoryResearchData AnalysisClinical researchInfectious diseasesCell CulturescienceLifesciencesELISAStatisticsSPSSPCRQualitative ResearchEpidemiologyGeneticsLife Sciences

Skills and Expertise

Self Assessment :
Analytical skills Build and manage the Trial Master File (TMF) Create SOPs Interact with nurses Interact with physicians Interpret data Monitor a clinical study Report dataAdminister logisticsAdministrative supportAdvise on strategyArchive documentationArchive study documentsArchive trial documentation and correspondence.Assist study siteAssist with site training


  • Master of Science (MSc) in Epidemiology and Biostatistics from JOOUST in 2016
  • Biomedical Science and Technology in Laboratory Medicine from Maseno University in 2006


BrightOwl Assessment:
Self Assessment:
Professional Proficiency

Work Preferences

  • Notice Period:
    4 weeks
  • Positions I am interested in:
    Clinical Research Associate (CRA) Clinical Project Manager (CPM)
  • Work From Home:
  • Work Regime:
    Permanent position
    BrightOwl freelancer
  • International:

Area / Region

Nairobi, Nairobi County, Kenya


Driving License
  • Yes