Clinical Research Coordinator - Turnhout
Core
Support clinical trial execution at a site in Turnhout through administrative and clinical coordination tasks.
Role type
Clinical Research Coordinator
Builds
Clinical trial operations and data integrity for life sciences research
Domain
Clinical research / Life sciences
Required skills
Clinical trial protocols, patient screening, informed consent, EDC systems, IRT/IWRS systems, medical terminology, MS Office, study documentation management
Preferred skills
Experience as Research Nurse or Clinical Research Assistant
Technologies
EDC systems, IRT/IWRS systems, MS Office (Outlook, Word, Excel, Access)
Responsibilities
Prescreening and screening patients, reviewing site database charts, maintaining study documentation (protocols, CRFs, eTMFs), supporting patient enrollment and consent, processing and shipping lap samples, managing investigational product inventory, coordinating study procedures, communicating with study monitors
Seniority
Mid-level, hands-on IC