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i am interested in clinical research and my experience as a former medical Sales representative has boosted this interset in me.

my Training and experience exposed me to: monitoring visit, assisting clinical teams in preparation...

therefore i am assured that all these exposures and experiences with the medical line will be of great use if you consider me for Clinical Research Associate in your establishment.

the position of CRA côte d'ivoire/ burkina faso really interest me because of my working experience and relations in côte d'ivoire (1999-2001). in addition i studied Pharmacy in burkina faso between (1992-1995) and i believe this will be an added advantage to me concerning the familiarity and adaptation to the country's environnemental condition.

i want to add that i am having a French passport that can aqually facilitate any travelling that my working in your establishment might require.

working in your company as CRA will be a great honour

i am looking forward in anticipation of favourable response

yours faithfully


Past Experience

  • Medical Sales Representative Neuilly-sur-Seine, France

    January 2015 --- December 2015


Self Assessment :
AdaptabilityAttention to detailCollaborationCommunicativeCreative thinkingCritical thinkingCuriosityDependabilityEfficiencyFlexibilityIndependenceInterest in knowledgeOrganizationProactivityResponsibilitySociabilityStrategic thinkingSelf-discipline


Self Assessment :
DiabetesClinical monitoringClinical researchClinical study reportsClinical trialsCommercializationCommunication SkillsDrug Safety and PharmacovigilanceEndocrinologyEnglishGood Clinical Practice (GCP)Marketing CommunicationsMarketing StrategyMicrosoft ExcelMicrosoft PowerpointMicrosoft OfficeMicrosoft WordOpthalmologyPatient Follow UpPatient recruitmentPatient Reported Outcome Measures (PROMs)Patient Screening and RecruitmentPharmaceutical IndustryPharmaceutical sales

Skills and Expertise

Self Assessment :
Approve suitability of patient information and consent documentsApprove queriesApprove patient informationApprove monitoring reportsArchive study documentsArchive trial documentation and correspondence.Archive documentationAttend seminars, courses and meetings within and outside the companyAssure medical qualityBuild trial master file (TMF)Collaborate with medical teamCollect patient forms and questionnaires Build and manage the Trial Master File (TMF) Design case record forms Develop clinical trial protocols Develop protocols Interact with physicians Monitor a clinical studyComplete case report form (CRF)Complete study proceduresCommunicate with investigatorCommunicate with sponsorConduct site initiationManage clinical trial files/documentsManage trial master file (TMF)


  • clinical research associate certificate in Pharmaceutical Engineering from FOR DRUG CONSULTING in 2014

Training and Certification

  • CRA Certificate in 2014 Certification
  • medical sales representative in 2005 Certification
  • Baccalaureat in 1998 Certification


BrightOwl Assessment:
Self Assessment:
Full Proficiency
Professional Proficiency
Elementary Proficiency

Work Preferences

  • Positions I am interested in:
    Clinical Research Associate (CRA)
  • Locations I am interested in:
  • Work From Home:
    Yes, 0 to 5 days per week
  • Work Regime:
    Permanent position
    BrightOwl freelancer
    BrightOwl employee
  • International:

Area / Region

Gisors, France


Driving License
  • Yes

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