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Summary

i am currently working as a Clinical Research Consultant for xpe pharma & science, who has outsourced me for the pfizer clinical research unit in anderlecht from the start of my Career. my current role as a clinical research recruiter (both healthy volunteers and Patient Recruitment) is a great fit with my personality as i am an enthusiastic, dedicated, dynamic, organized and social person with strong trilingual Communication and Leadership skills. specialties: // clinical research // science)" rel="nofollow">Protocol reviews // Phase I clinical studies // icd reviews // Volunteer recruitment // data collection // SOP // ich gcp knowledge // networking // process Innovation & optimalization // trilingual (dutch - French - English)

Experiences

Current Experience

  • Clinical Research Consultant

    Anderlecht, Belgium
    Since February 2015
    i am currently working as a Clinical research recruiter within the pfizer Clinical research unit (pcru). the pcru mainly focusses on Phase I Drug Development, which means i am familiar with the different phases of Clinical trials and Drug Development. being a Clinical research recruiter, i have a broad range of responsibilities: • recruit the right amount of healthy volunteers and/or patients matching the recommended in- and exclusion criteria mentioned in a study specific science)" rel="nofollow">Protocol. • recruit volunteers within our existing database and by advertisements and Social Media. • i am continuously trying to improve and implement my strategies in order to achieve my goals. • overall study organization, which results in a close collaboration with all other departments. I am currently working as a clinical research recruiter within the Pfizer Clinical Research Unit (PCRU). The PCRU mainly focusses on phase I drug development, which means I am familiar with the different phases of clinical trials and drug development. Being a Clinical Research Recruiter, I have a broad range of responsibilities: • Recruit the right amount of healthy volunteers and/or patients matching the recommended in- and exclusion criteria mentioned in a study specific protocol. • Recruit volunteers within our existing database and by advertisements and social media. • I am continuously trying to improve and implement my strategies in order to achieve my goals. • Overall study organization, which results in a close collaboration with all other departments.

  • Clinical Research Nurse


    Since January 2014
    i am responsible for the datacollection and the general safety of trial subjects during phase 1 Clinical Trial studies. I am responsible for the datacollection and the general safety of trial subjects during phase 1 clinical trial studies.

Past Experience

  • Informer for Hyundai

    January 2015 --- January 2015

  • Nurse (Student job)

    September 2013 --- January 2014
    o maternity o Pediatrics o revalidation o Nephrology

  • Midwife (intern)

    March 2013 --- May 2013

  • Midwife (intern)

    September 2012 --- September 2012

  • Midwife (intern)

    January 2011 --- September 2012

  • Midwife (intern)

    March 2011 --- April 2011

Personality

BrightOwl Assessment :
CommunicativeCollaborationCharmAttention to detailDependabilityFlexibilityOrganizationStrivingAnalytical thinkingPerspective

Knowledge

BrightOwl Assessment :
Diabetes Phase IClinical researchPharmaceutical IndustryElectrocardiogram (ECG)ObstetricsPediatricsInformed Consent ProcessClinical trialsPatient Screening and RecruitmentPatient Follow UpStudy approvalsSafety reportingTranslation
LinkedIn Assessment :
ObstetricsEnglishFrenchdutchPresentationsClinical researchPediatricsHospitalsClinical DevelopmentRegulatory affairsLife Sciences

Skills and Expertise

BrightOwl Assessment :
Write protocolsCollect dataReview informed consent processUnderstand protocolsReview protocolsCommunicate with investigatorPrepare regulatory documentsEstablish contracts

Education

  • Bachelor's Degree in Direct Entry Midwifery from Erasmushogeschool Brussel in 2013
  • High School in Economics-Languages from Sint-Martinus Overijse in 2009

Languages

BrightOwl Assessment:
Dutch
Native
French
Native
English
Full Proficiency
Self Assessment:

Area / Region

Brussels, Belgium

Others

Driving License
  • No

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