CareerPlan

Zdravotní sestra pro klinické studie

Prague, CzechiaFull-time2026-03-26 → 2026-11-12

Core

Conducts multiple clinical trials of varying sizes and complexity for patients and healthy volunteers, ensuring data quality, participant safety, and protocol adherence.

Role type

Clinical Research Nurse (CRN)

Builds

Clinical trial data and patient safety records

Domain

Healthcare / Clinical Research

Required skills

Clinical nursing practice, GCP/ICH compliance, vital signs monitoring, EKG, phlebotomy, adverse event reporting, participant recruitment and retention, data documentation

Preferred skills

Experience with investigational product (IP) handling, administrative tasks in clinical settings

Technologies

MS Office

Responsibilities

Conduct clinical study procedures (screening, vitals, EKG, blood draws) per protocol; ensure participant safety and comfort; maintain accurate data documentation; report protocol deviations and adverse events; support participant recruitment and retention; manage IP storage and dispensing if needed; attend study meetings and training.

Seniority

Mid-level, hands-on IC