Zdravotní sestra pro klinické studie
Core
Conducts multiple clinical trials of varying sizes and complexity for patients and healthy volunteers, ensuring participant safety, data quality, and protocol adherence.
Role type
Clinical trial nurse (IC)
Builds
Clinical trial operations and participant care
Domain
Healthcare / Clinical Research
Deliverable
physical/clinical work
Required skills
Clinical trial protocol execution, vital signs monitoring, EKG administration, phlebotomy, adverse event reporting, participant recruitment and retention, regulatory compliance (GCP/ICH), data documentation
Preferred skills
Investigational product handling, multi-tasking in clinical environments
Technologies
MS Office
Responsibilities
Conduct clinical study procedures per protocol (screening, vitals, EKG, blood draws), ensure participant safety and comfort, maintain accurate trial documentation, report protocol deviations and adverse events, support participant recruitment and retention, manage investigational product storage and dispensing when needed
Seniority
Mid-level, hands-on IC