BrightOwl Loader Loading

Experiences

Current Experience

  • Clinical Research Coordinator


    Since December 2012
    • coordination and conduction of sixteen Clinical trials • management of sixteen different protocols, participant tests and procedures • collaboration with principal investigators, Pharmacy staff, medical staff, patients and sponsor • preparation and submission of protocols and amendments • supporting principal Investigator to ensure that patients are eligible, to screen and enroll patients in studies • assisting principal Investigator in Communication of study requirements to all individuals involved in the study • execution of study design and science)" rel="nofollow">Protocol requirements • Clinical trials management: recruitment of patients, inclusion/exclusion criteria, icf, ae recording, concomitant medications recording, ivrs system, collection of data and source documents, drug administration, drug accountability, collection of blood samples, Treatment of Lab samples (blood + urine) • Data Management: monitorings, audits, queries, sae reports, ecrfs completion • Coordination and conduction of sixteen clinical trials • Management of sixteen different protocols, participant tests and procedures • Collaboration with Principal Investigators, pharmacy staff, medical staff, patients and sponsor • Preparation and submission of protocols and amendments • Supporting Principal Investigator to ensure that patients are eligible, to screen and enroll patients in studies • Assisting Principal Investigator in communication of study requirements to all individuals involved in the study • Execution of study design and protocol requirements • Clinical trials management: recruitment of patients, inclusion/exclusion criteria, ICF, AE recording, concomitant medications recording, IVRS system, collection of data and source documents, drug administration, drug accountability, collection of blood samples, treatment of lab samples (blood + urine) • Data management: monitorings, audits, queries, SAE reports, eCRFs completion

Past Experience

  • Master's thesis

    October 2009 --- June 2011
    « role of mir-802 in embryonic pancreas »

  • Bachelor’s thesis

    January 2008 --- March 2008
    « setting up of extraction of fetal DNA from maternal circulating blood and PCR conditions »

  • Intern

    July 2007 --- July 2007

Knowledge

LinkedIn Assessment :
molecular biologyBioinformatic toolsAnimal manipulationCell biologyMicroscopyLifesciencesHistologyCell CultureICH-GCPClinical researchClinical trials

Education

  • in Certificate in GCP for Investigator Site Teams & Ethics Committees from FormaliS in 2015
  • Certificate in Good Clinical Practice in from BioWin (Seneffe) in 2013
  • Certificate in ICH - GCP Refresher in from European Centre for Clinical Research Training (ECCRT) in 2013
  • in Certificate in Laboratory Animals Science (FELASA C) from Université catholique de Louvain in 2011
  • Master in Biomedical Sciences - Molecular and Cellular Biology in from Université catholique de Louvain in 2011
  • Bachelor in Medical Biology in from Institut Paul Lambin in 2008

Area / Region

Brussels, Belgique

Others

Driving License
  • No

Similar Candidates

Other Candidates in Belgium

Other Candidates in Brussels

Other similar Candidates in Brussels

Other Candidates

Most Recent Searches

Most Famous Searches

You might also like