Clinical Research Coordinator - Bydgoszcz
Core
Support clinical trial execution at a research site in Bydgoszcz by managing patient screening, documentation, and investigational product logistics.
Role type
Clinical Research Coordinator
Builds
Clinical trial data and patient enrollment
Domain
Life sciences / Clinical research
Required skills
Clinical trial protocols, IRT/IWRS systems, lab sample handling, medical terminology, MS Office, patient screening, informed consent management, study documentation, IP accountability
Preferred skills
None stated
Technologies
IRT/IWRS, EDC systems, eTMFs, EMR
Responsibilities
Prescreening and screening tasks, reviewing charts from site database, maintaining study documentation, supporting patient enrollment, managing IP inventory and randomization, processing lab samples, coordinating study procedures, communicating with study monitors
Seniority
Mid-level, hands-on IC