ambitious, enthusiastic and eager to learn Clinical Research Coordinator, wants to continue to grow within the field of clinical research. has experience in performing several different clinical studies. is well able to work in a team and can adjust and adapt in changing cultures and working environments. has excellent Communication Skills, in written and spoken English and dutch. is independent, precise and a real 'troubleshooter’. has learned to work according to the Good Clinical Practice guidelines, by the (co) establishing of various studies. can motivate both children as well as adults in a natural way. has perseverance and can really ‘get into’ at a topic under the incentive that giving up is not an option .
Clinical Research CoordinatorVelp, Nederland
Since August 2013
responsible for the proper implementation of, and Compliance with, several research protocols in the field of cardiovascular disease. setting up Phase II - iv studies from initiation until close-out. responsible for the right transcription of source documents into eCRF’s and for resolving any queries. caused by my critical view being an important Member in the quality committee of andromed in creating and refreshing SOP’s. responsible for distributing of study documents to the right colleagues (pi, sub-i or research Nurse).
Responsible for the proper implementation of, and compliance with, several research protocols in the field of cardiovascular disease. Setting up phase II - IV studies from initiation until close-out. Responsible for the right transcription of source documents into eCRF’s and for resolving any queries. Caused by my critical view being an important member in the quality committee of Andromed in creating and refreshing SOP’s. Responsible for distributing of study documents to the right colleagues (PI, SUB-I or research nurse).
As a research coordinator thé contact point on behalf of the site in Velp for pharmaceutical companies, but also for patients. In this way, the crucial link link between theory and practice.
Research Assistant Amsterdam, NederlandNovember 2012 --- December 2012
Research Assistant ABCD study AmsterdamSeptember 2012 --- October 2012
assisted in performing tests in the olympic stadium in amsterdam in children between 8 and 10 years. these tests involved fitness and muscle strength measurements.
AdaptabilitySelf-disciplineProblem solvingOrganizationInterest in knowledgeIndependenceFlexibilityEfficiencyCritical thinkingCoordinationCharmService oriented
Diabetes Scientific writingCardiovascular diseasesClinical researchClinical Study DesignClinical trial audits and inspectionsClinical trialsEnglishGCPGood Clinical Practice (GCP)ICH GCP guidelinesInformed Consent ProcessMicrosoft OfficePowerPointPhases of clinical development (phase I to IV)ProtocolScientific WritingScreen patientsSerious Adverse Event (SAE)SOPWriting Study Procedures and SOPs
Skills and Expertise
Create SOPs Interact with nurses Interact with physicians Monitor a clinical study Search literature on clinical trials Write papersAdverse event reporting
Master in Movement Science from Maastricht University in 2012
Bachelor in Health Science from Maastricht University in 2011
Training and Certification
Emergency Response Officer in 2015 Certification
Good Clinical Practice in 2014 Certification
Expert has 1 publications (Will be avalible with full profile)