Clinical trial coordinator - trainerHasselt
Since October 2009
my academic background is that of master of Nursing science, while my professional experience has brought me to Clinical research and the Pharmaceutical Industry. i specialized in several areas, all closely linked: from Training in Clinical research to the management of projects together with pharma. whether it is a Training, moderating a meeting or contributing to the development of patient or Nurse materials, i am always up for a challenge that will get me thinking, learning and working in a team.
Flexibility is key. short projects, fast results.
My academic background is that of master of nursing science, while my professional experience has brought me to clinical research and the pharmaceutical industry. I specialized in several areas, all closely linked: from training in clinical research to the management of projects together with pharma. Whether it is a training, moderating a meeting or contributing to the development of patient or nurse materials, I am always up for a challenge that will get me thinking, learning and working in a team.
Flexibility is key. Short projects, fast results.
Clinical researchClinical trial managementClinical trialsGood Clinical Practice (GCP)Oncology Clinical ResearchOracle ClinicalPhases of clinical development (phase I to IV)Clinical monitoring
Skills and Expertise
Guide students Interact with nurses Interact with physicians Monitor a clinical study Report data Search literature on clinical trialsAdverse event reportingAssist study siteAssist with proceduresAssist with site trainingAttend at steering committee meetingsAttend investigator meetingAttend seminarsAttend seminars, courses and meetings within and outside the companyAttend steering committeeClinical data collectionCoachCoach 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.Communicate with investigatorCommunicate with sponsorCommunicationComplete case report form (CRF)Complete study proceduresConduct site initiationConduct studiesConduct the trialControl studiesCoordinate projectsCoordinate regular advisory boardCoordinate with the ethics commiteeData entryFacilitate sponsor monitoring visitsFollow up training programsGastrointestinal diseasesGuide studentsGuide staffInformed consent processInitiate clinical trials Interact with ethics committeeInteract with KOLInteract with nursesInteract with pharmacistsInteract with physiciansLiaise with doctors and other professionals throughout the studyOral presentationOrganise meetingsOrganise steering committeePrepare internal auditsPrepare external auditsTeachingTrain off site staffTrain on site staffTrain Staff
master in nursing from University of Leuven in 1989