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Summary

Holding a Medicine degree,I worked as a General Practitioner in a private sector and in hospitals for four years in Algeria . I also persued an one-year specialization in Radiodiagnosis.

After coming in belgium, I followed a 2-month training  in biothecnology ( culture in vivo).This training allowed me to work as lab assistant in a medical laboratory.

I have followed a 2-month training course  wich provides me the necessary background to perform within the clinical trial.

I am actually Assistant Project Manager at Biomedical Systems and I am looking for new challenges as Clinical Research Associate.

 

Experiences

Current Experience

  • Assistant Project Manager Auderghem, Belgium
    Since September 2015

    • Assists in the development of project proposals, cost estimates and budgets,

               timelines and schedules                                                

    • creating and implementing project work plans
    • revising plans details based on client needs and project requirements
    • reviewing reports prepared by staff before passing to the client
    • implementing company methodologies and project principles
    • overseeing quality assurance procedures
    • preparing project reviews and documenting project details
    • performing site training and support sites.

Past Experience

  • lab assistant
    December 2013 --- January 2015
    • General biochemical blood and urine tests. • Special biochemical blood and urine tests. • Biochemical tests on biological liquids (pleural, synovial, peritoneal, cerebrospinal) • Determination of specific proteins. • Drug monitoring. • Microscopy of urine sediments and biological liquids

  • stage de perfectionnement sur les differentes techniques de PCR
    October 2013 --- October 2013
    Théorie : PCR (module avancé) : préparation des échantillons, notions de Real time PCR, technologie de séquençage, mutagenèse dirigée Pratique : - PCR appliquée aux tests diagnostic, PCR Triplex (détection de germes MRSA, détection d’affections génétiques) - Technique de Real Time PCR

  • Resident doctor in medical radiology
    November 2012 --- June 2013

    • Practicing ultrasounds, telethorax, plain radiographs, CT scans 

  • Medecin generaliste
    November 2010 --- April 2011

    • Provide medical care and conduct wellness exams for

    individuals and medicare beneficiaries

    • Provide education for the prevention of serious diseases and

    assist patients in the management of acute and chronic

    medical conditions

    • Diagnose patients, order diagnostic tests and provide

    referrals for specialized treatment or rehabilitation

    • Determine cause of sickness and prescribe medications
    • Collaborate with clinical staff and specialty Physicians on
    • multiple discipline treatments and coordinated care efforts
    • Strong knowledge of relevant drugs, chemical compositions

    and substance properties

  • Medecin generaliste
    April 2009 --- February 2010

    • Provide medical care and conduct wellness exams for

    individuals and medicare beneficiaries

    • Provide education for the prevention of serious diseases and

    assist patients in the management of acute and chronic

    medical conditions

    • Diagnose patients, order diagnostic tests and provide

    referrals for specialized treatment or rehabilitation

    • Determine cause of sickness and prescribe medications
    • Collaborate with clinical staff and specialty Physicians on
    • multiple discipline treatments and coordinated care efforts
    • Strong knowledge of relevant drugs, chemical compositions

    and substance properties

  • medecin generaliste
    November 2008 --- March 2009

    • Provide medical care and conduct wellness exams for

    individuals and medicare beneficiaries

    • Provide education for the prevention of serious diseases and

    assist patients in the management of acute and chronic

    medical conditions

    • Diagnose patients, order diagnostic tests and provide

    referrals for specialized treatment or rehabilitation

    • Determine cause of sickness and prescribe medications
    • Collaborate with clinical staff and specialty Physicians on
    • multiple discipline treatments and coordinated care efforts
    • Strong knowledge of relevant drugs, chemical compositions

    and substance properties

Personality

Self Assessment :
AdaptabilityFlexibilityEfficiencyCuriosityCreative thinkingCoordinationCompetitivenessAuthenticityAttention to detailAssertivenessAnalytical thinkingInterest in knowledge

Knowledge

Self Assessment :
Diabetes Labtechnician Medical devices Phase I Scientific writing R&DAnesthesia NegotiationA rising single dose tolerance studyAntibodiesCancerBiological Drug DevelopmentBiopharmaceuticalsBiotechnologyCardiovascular diseasesCardiologyCell CultureClinical DevelopmentClinical pharmacologyClinical researchClinical monitoringClinical trialsCommunication SkillsData entryData ManagementDermatologyDiagnostic radiologyData AnalysisDrug InteractionDrug metabolismDrug regulatory authoritiesDrug Safety and PharmacovigilanceEmergency medicineActions and modes of action of drugs in the human species Lab scale batchesEnzyme-linked immunosorbent assay (ELISA)GastroenterologyEnglishGCPGood Laboratory Practice (GLP)GMPEthics submission and approval processHematologyKnowledge of the drug development processVaccinesUnderstanding of regulatory guidelinesSerious Adverse Event (SAE)SOPSafety trialsRheumatologymedical radiologyoncologyRadiation oncologyradiotherapyProject Management
LinkedIn Assessment :
MarketingSocial NetworkingmanagementEnglishSocial MediaOnline AdvertisingDrug SafetypharmacogilancePublic Relations

Skills and Expertise

Self Assessment :
Analyze data Assure medical quality Build and manage the Trial Master File (TMF) Build the CMC development plan Control data Interact with nurses Interact with physicians Interpret dataAdjust methods Develop protocols Monitor a clinical study Receptor Pharmacology Report data Search literature on clinical trialsAdvise on medical perspectives Lab scale batches Use content management systems Technology researchAdministrative supportAnalyze dataApprove patient informationAssess adverse reactions Develop clinical trial protocolsAssess subject safetyArchive documentationApprove monitoring reportsAssist study siteAttend seminarsAssure medical qualityAssist with proceduresCapture data on source documentsClinical data collectionCollaborate with medical teamConduct post-marketing surveillance studyComplete case report form (CRF)Communicate with investigatorConduct close-out visitsConduct literature searchesCoordinate with the ethics commiteeDocument adverse eventsData verificationDesign inclusion criteriaDesign information leafletDesign exclusion criteriaFacilitate sponsor monitoring visitsIndentify clinicians to conduct clinical trialsIdentify investigatorsInteract with CROsInteract with nursesInitiation visitInteract with physiciansIndentify sitesradiological assesment of tumorsradiological softwaresCRFQAmedical information

Education

  • professional training in clinical trials from Clinet-cefochim in 2015
  • professionnel training in Biotechnology from culture in vivo in 2013
  • doctorat in Medecine generale from Faculté de medecine -Blida-Algerie in 2008

Training and Certification

  • Expert in Clinical Trials in 2015 Certification
  • Biothechnology in 2013 Certification

Languages

BrightOwl Assessment:
Self Assessment:
French
Native
English
Full Proficiency
Arabic
Native
Dutch
Elementary Proficiency
German
Elementary Proficiency

Work Preferences

  • Notice Period:
    4 weeks
  • Locations I am interested in:
  • Work From Home:
    No
  • Work Regime:
    Permanent position
    BrightOwl employee
  • International:
    Yes

Area / Region

Namur, Belgium

Others

Driving License
  • Yes