Clinical Research Coordinator - Mariánské Lázně
On-site
Core
Support clinical trial execution at a site in Mariánské Lázně by managing documentation, patient screening, data entry, and sample logistics.
Role type
Clinical Research Coordinator (Site Research Assistant)
Builds
Clinical trial data and patient enrollment
Domain
Clinical research / Life sciences
Required skills
Clinical trial protocols, medical terminology, EDC systems, data entry, sample shipping, MS Office, patient screening, informed consent management
Preferred skills
None stated
Technologies
EDC systems, MS Office (Outlook, Word, Excel, Access)
Responsibilities
Maintain study documentation (protocols, CRFs), support patient screening and enrollment, coordinate study procedures, perform data entry and quality checks, manage biological sample shipping, communicate with study monitors
Seniority
Mid-level, hands-on IC