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Biologist looking for environment/nature/science related job close to home.


Current Experience

  • Clinical Data Manager (DM)

    Since April 2006
    Clinical Research Physician · Develop the data management sections of the clinical trial protocol · Assist in final review of the clinical trial protocol for consistency · Define & create the database (in-house created software) · Develop (paper and electronic) Case Report Forms in accordance with the protocol and the database (in-house created software) · Develop guidelines for Case Report Forms completion · Create randomization program (in-house created software) · Develop cross check programs for consistency and validation checks on the data (in-house created software) · Coordinate and control data collection, data cleaning and data reporting activities · Communicate with participants in order to resolve queries and outstanding data sending · Develop and maintain update and validation plans for the studies · Prepare reports on the studies under my responsibility · Assist the Statistician during interim / final analysis · Organize the preparation and execute the review with the Study coordinator/Clinical Research Physician on a regular basis

Past Experience

  • Voluntary practicals' assistant Antwerp

    October 2003 --- September 2005

  • Sciences & Maths teacher

    November 2000 --- September 2004

  • Voluntary researcher Mechelen

    May 2001 --- August 2001


BrightOwl Assessment :
Impulse commandInterest in knowledgeEfficiencyDependabilityOrganizationAdaptabilityApproachabilityAssertiveness
Self Assessment :
EfficiencyTrustInterest in knowledgeApproachabilityAttention to detailAuthenticitySociabilityAssertivenessIndependenceDependability


BrightOwl Assessment :
Medical oncology Data entryData ManagementClinical Data Management (CDM)Validation
Self Assessment :
Randomization and blindingPhases of clinical development (phase I to IV)Developing Clinical Trial ProtocolsDesigning case report formsClinical trial designDatabase design and maintenanceData entryInformed Consent ProcessPhenotype Scientific methodologyClinical researchICH-GCPData ManagementEnglishFrenchdutchscienceBiologyZoologyEthology/animal behaviourEnvironmentSustainable developmentAnimal Welfare
LinkedIn Assessment :
Clinical trialsData ManagementClinical researchClinical Data Management (CDM)CancerValidationICH-GCPBiologyZoologyMarine BiologyAnimal BehaviorAnimal WelfareEthologyWildlife BiologyAnimal CareWildlife ConservationConservation Biology

Skills and Expertise

BrightOwl Assessment :
Analyze data/information to determine potential relationships.assess the needs of the project(s)/program(s) and make changes in process, work flow and/or assignments.Collect data as required by the protocol and complete case report forms and reviews for completeness.Coach and provide guidance to clinical staff.Conduct limited data and/or statistical analysis.control different protocol versions and other essential documents
Self Assessment :
Publish scientific projectsAnalyze data/information to determine potential relationships.Build and manage the Trial Master File (TMF)collaborate in research projects at universitiesConduct literature searches.Conduct limited data and/or statistical analysis.Design the database Design, document, test, implement and manage clinical data collection and reporting systemsEnsure consistency between the protocol and CRFLiaise with research team in order to accurately collect and record dataLiaise with professionals in other divisions of the company as requiredLiaise with doctors and other professionals throughout the studyPerform investigative site file reconciliation: requests any new and updated site-related essential and non-essential documents and reviews them for content, consistency with other documents, and compliance with appropriate local regulatory requirements, ICH guidelines, project Standard Operating Procedures (SOPs), and sponsor requirements.Prepare medical reportsSupport oral and written presentations of clinical results by study investigators.Teach university studentsWork collaboratively with the other members of the clinical research team DesignOrganizeexecute and publish scientific projects (in biology)'Designexecute and publish scientific projects (in biology)'Design scientific projects (in biology)Organize scientific projects (in biology)Execute scientific projectsPublish scientific projects


  • Master in Applied Animal Behaviour & Animal Welfare from Edinburgh University in 2002
  • Master in Biology - Zoology from Ghent University in 2000
  • High school in Science and mathematics from Sint Laurensinstituut Zelzate in 1996


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

Work Preferences

  • Notice Period:
    12 weeks
  • Locations I am interested in:
    Aalst, Belgium Dendermonde, Belgium Erpe-Mere, Belgium Geraardsbergen, Belgium Ghent, Belgium Lokeren, Belgium Melle, Belgium Ninove, Belgium Oudenaarde, Belgium Wetteren, Belgium Zottegem, Belgium
  • Work From Home:
    Yes, 0 to 5 days per week
  • Work Regime:
    Permanent position :    I'm currently working 4/5, which combines perfectly with my family life, so I would like to continue this schedule in the future.% FTE
    BrightOwl employee :    I'm currently working 4/5, which combines perfectly with my family life, so I would like to continue this schedule in the future.% FTE
  • International:


    Expert has 1 publications (Will be avalible with full profile)

Area / Region



Driving License
  • Yes

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