Requirements: English
Company: IQVIA
Region: Nijmegen , Gelderland
IQVIA is currently recruiting for a Clinical Research Coordinator to support a site in Venlo. This role with an immediate start is for 32 hours per week and is expected to last until around the end of the year. The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies, under the direction and delegation of the Principal Investigator. As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support the clinical trial team and ensure the smooth running of the clinical trial, including: Maintaining up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents Planning and coordinating logistical activity for study procedures according to the study protocol Data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness Administrative research task BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.G. clinical research coordinator, Research Assistant, nurse, medical assistant, other medical profession Basic knowledge of medical terminology Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word Fluent Dutch language skills