Looking for a challenging job with growth potential in biotechnological, biomedical or pharmaceutical sector. Important personal values are: working in a team, lifelong learning and contributing to a better society.
Clinical Trial Assistant (CTA)
Since October 2014
Administrative and logistical support of CRAs in monitoring hospital staff during a clinical study. The main tasks are: communication with hospital staff, payments to physicians/patients and maintaining of the clinical files.
Records Management Associate
April 2014 --- September 2014
Controlling, completing and archiving of clinical files according to ICH-GCP guidelines. Final purpose is to constitute a complete file in order to present it to the FDA for the approval of a new medicine.
Analytical thinkingOrganizationProblem solvingCritical thinkingService orientedInterest in knowledgeAttention to detailFlexibilityReaction to stressIndependence
EnglishClinical trials Phase IClinical researchCTMSGood Clinical Practice (GCP)Quantitative PCR (qPCR)
Skills and Expertise
Write papersAdministrative supportArchive study documentsCollaborate with medical team Interact with nurses Interact with physiciansManage Clinical Trial Management System (CTMS) Manage trial master file (TMF)Financial administrationInteract with pharmacistsDistribute trial suppliesEnsure good clinical practice (GCP)lifescienceSolve problems
Master of Science (MSc) in Bioengineering sciences: cell and gene biotechnology from UGent in 2014
Bachelor of Science (BSc) in Bioengineering from Universiteit Antwerpen in 2011
Training and Certification
Introduction to ICH-GCP guidelines in 2014 Training