Lieve Vrints went to the University of Antwerp  and completed 6 years of Medical School.  

Her Clinical Research carrier started 20 years ago as Project Manager for the clinical trials conducted at the department of Urology/Oncology in a hospital in Antwerp.  

Afterwards she started working as Senior CRA, Lead CRA, Project Manager and Line Manager. After the switch in 2017 to freelance consultant, Lieve continued her carrier as Principal CRA, Project Manager, Site Liaison Lead, Sponsor Oversight Lead, Quality Assurance Specialist, Trainer and Auditor.  

Her goal and passion is to provide high-quality clinical research services to clients in the pharmaceutical and biotechnology sectors in combination with an extensive knowledge and expertise in conducting clinical trials in various therapeutic areas and phases, following ICH-GCP and ALCOA+ principles, complying with federal and local regulations. 
 
Lieve core competencies include clinical research auditing, pre-audit visits, internal and external site audits, quality control, site management, on-site monitoring, SOP development, training and supervision, ensuring the quality and integrity of the clinical data and processes.  

Her mission and determination is to support the development and approval of innovative and safe treatments that can improve the lives of patients worldwide.