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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

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