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Current Experience

  • study site coordinator/clinical research assistant
    Since February 2016
    Management of post-marketing studies medical devices in cardiovascular: - key contact for studies - provide administrative support to the research team - maintenance of records and regulatory documents - assist with enrollment of patients on assigned studies - coordinate data collection

Past Experience

  • study site coordinator/clinical research assistant
    April 2012 --- December 2015
    Management of international and national clinical studies dedicated to multiple sclerosis and devic disease- Phase II to IV and epidemiological -Therapeutic areas: neurology, ophtalmology, pediatrics - key contact for studies between investigators, internal departments, CRO, sponsors and vendors. - support investigators and coordinate clinical trials: Between 15 and 20 studies (from feasability to clos-out) - monitoring between 100 and 120 patients: prescreening, patients care, patients enrollment, data collection/CRF completion,investigational product dispensation, serious adverse event reporting / pharmacovigilance… - Protocols and GCP training of medical and non-medical staff (doctors, nurses, secretaries, radiologist, pharamacist, MRI technicians, lab technicians…) - Administrative management of clinical studies (feasibilities responses, Hospital contracts and extra costs, Billings establishment) - Maintenance and storage of administrative, regulatory and study related documents

  • epidemiological research associate
    August 2011 --- January 2012
    - Pathologies: rheumatoid arthritis and Crohn's disease - Selection of investigator for epidemiological studies - site initiation via phone call - administrative tasks

  • Internship lab technician biochemistry / biology
    February 2010 --- June 2010


Self Assessment :
AdaptabilityAnalytical thinkingAssertivenessApproachabilityAttention to detailAuthenticityCollaborationCommunicativeCoordinationCuriosityFlexibilityInterest in knowledgeOrganizationOptimismProactivityProblem solvingResult OrientedResponsibilityService orientedSociabilitySelf-discipline


LinkedIn Assessment :
Life SciencesPharmacovigilanceClinical DevelopmentMedical DevicesICH-GCPCROmanagementNeurologyOphtalmologyCoordinationPediatricBPCICHClinical researcheCRFIATA certificationLife Science IndustryClinical trialsBiotechnologyPharmaceutical IndustryCommunicationSense of prioritiesOrganisation skillsMS Office softwareEDCCustomer-focused ServiceAt Multitaskinganalytical approach and anticipation of problemsGCP

Skills and Expertise

Self Assessment :
Control data Interact with nurses Interact with physiciansAdminister, maintain and co-ordinate the logistical aspects of clinical trialsAnswer, transfer and handle incoming calls as needed.Archive study documentsArchive trial documentation and correspondence.Clinical data collectionCoach and provide guidance to clinical staff.Coach clinical staffCollaborate with medical teamCollaborate with PI and institution to respond to any audit findings and implement-approved recommendations.Collect dataCollect financial data from hospitalsCollect patient forms and questionnairesCommunicate effectively on different company levelsCommunicate with investigatorCommunicate with sponsorCommunicationCompile informationCollaborate with project teamComplete study proceduresConduct maintenance visitsConduct studiesConduct supply issue resolution activitiesContact potential subjectsConfirm protocol compliancecontrol different protocol versions and other essential documentsCoordinate projectsCoordinate logisticsCoordinationCreate clinical documentsCreate study documentsCreates a collaborative team environmentData verificationDesign tracking systemDocument employees training requirementsEnsure good clinical practice (GCP)Estimate subject complianceFacilitate sponsor monitoring visitsIdentify and provide training to trial team and associated staffInteract with CROsInteract with computer specialistsInteract with nursesInteract with pharmacistsInteract with physiciansLiaise with doctorsLiaise with doctors and other professionals throughout the studyLiaise with professionals in other divisions of the company as requiredLiaise with research team in order to accurately collect and record datalifescienceManage clinical suppliesManage clinical trial files/documentsManage multiple projectsMonitoring subject complianceNegotiate protocol details Negotiate payment schedulesOffice managementOversee data collectionPatient recruitmentPersuade clinicians to conduct clinical trialsPlan work to meet objectives and deadlinesSchedule trial visitsScreen patientsShipment of biological specimenWork with coordination and data management teamsWork collaboratively with the other members of the clinical research team


  • DIU FARC-TEC in Clinical Research Coordinator from Claude Bernard Lyon 1 university in 2012
  • Master 1 Degree in Biochemistry Engineering and Biotechnologies from Claude Bernard Lyon 1 university in 2011
  • Bachelor's degree in in Biology and Biochemistry from Claude Bernard Lyon 1 university in 2008


BrightOwl Assessment:
Self Assessment:
Professional Proficiency
Elementary Proficiency

Area / Region

Lyon, France


Driving License
  • No