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Summary

Clinical Trial Coordinator

Experiences

Past Experience

  • Senior Clinical Trial Assistant (CTA) Lubbeek, Belgium

    November 2016 --- November 2018

  • Clinical Trial Coordinator - Fern Valley Consultant Diegem

    March 2013 --- September 2016
    Project Leader

  • Clinical Safety Officer Assistant via Valesta

    April 2010 --- March 2013
    Adverse Events

  • Clinical Project Assistant via Valesta

    March 2012 --- November 2012
    Clinical

  • Pharmacovigilance Assistant via Valesta

    September 2008 --- April 2010
    Adverse Events

  • Assistant, Drug Supplies, Labeling and Site Documentation – Regulatory Affairs and Quality Assurance

    October 2007 --- September 2008
    Clinical Trial

  • Data Coordinator – Investigator Services

    March 2006 --- October 2007
    Laboratory

Personality

BrightOwl Assessment :
Anger commandImpulse commandPerspectiveOrganization
Self Assessment :
OptimismSociabilityInterest in knowledgeWillingness to compromiseAttention to detail

Knowledge

BrightOwl Assessment :
Principles and ethics of clinical researchscienceLife SciencesMultilingualPhases of clinical development (phase I to IV)ProtocolProject ManagementTeamwork
Self Assessment :
Cardiovascular diseasesEndocrinology and metabolismPhases of clinical development (phase I to IV)Clinical trial designRandomization and blindingDrug development processICH GCP guidelinesInformed Consent ProcessClinical researchElectronic Data Capture (EDC) EnglishClinical trialsMedical DevicesCTMS
LinkedIn Assessment :
PharmacovigilanceRegulatory affairsClinical researchQuality Assurance (QA)Software DocumentationProject ManagementCTMSPharmaceutical IndustryCROClinical DevelopmentClinical monitoringElectronic Data Capture (EDC) oncologyRegulatory submissionsTherapeutic AreasSOPCardiologyClinical Data Management (CDM)Diabetes

Skills and Expertise

BrightOwl Assessment :
Identify and provide training to trial team and associated staffCreates a collaborative team environmentWork collaboratively with the other members of the clinical research team Act as the main line of communication between the sponsor and the investigatorCollaborate with PI and institution to respond to any audit findings and implement-approved recommendations.Calculate timelines for conducting and completing the trialCoach and provide guidance to clinical staff.
Self Assessment :
Answer, transfer and handle incoming calls as needed.Perform administrative support duties as requiredperform data entryPlan work to meet objectives and deadlinesprepare study-related documentation; Provide general office management to keep operations running smoothly.Submit regulatory applicationsUpdate Clinical Trials Management System (CTMS) Archive trial documentation and correspondence.Assemble regulatory applicationsWork collaboratively with the other members of the clinical research team

Education

  • postgraduate in Diabeteseducator from Artevelde Hogeschool Gent in 2006
  • Bachelor in Nutrition and Dietetics from Plantijnhogeschool van de provincie Antwerpen in 2005
  • in from Lessius Hogeschool Antwerpen in 0000

Languages

BrightOwl Assessment:
Self Assessment:
Dutch
Native
English
Professional Proficiency
French
Elementary Proficiency

Work Preferences

  • Locations I am interested in:
    Leuven, Belgium
  • Work From Home:
    Yes, 0 to 1 days per week
  • Work Regime:
    Permanent position :    80% FTE
    BrightOwl employee :    80% FTE
  • International:
    No

Area / Region

Kessel-Lo, Belgium

Others

Driving License
  • Yes

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