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Clinical Research Nurse

Prague, Czechia💼 Full-time🗓 2026-04-01 → 2026-07-31

Core

Conducts clinical trials involving patients or healthy volunteers, ensuring subject safety and data capture per study protocols.

Role type

Clinical Research Nurse (Site Coordinator)

Builds

Clinical trial operations for pharmaceutical/biotech sponsors

Domain

Clinical Research / Healthcare

Deliverable

physical/clinical work

Required skills

Clinical trial conduct, patient safety monitoring, data documentation, study recruitment, regulatory compliance (FDA/GCP/ICH), medical assessments, adverse event reporting, team mentoring

Preferred skills

English fluency, independent analysis, problem solving, negotiation, organizational skills

Technologies

Computer applications, clinical trial software

Responsibilities

Conduct clinical studies per FDA/GCP guidelines, provide medical care to patients, schedule subject visits, perform study activities (informed consent, screening, vital signs, labs), record patient data, report non-compliance, obtain IRB approval, monitor participant safety, serve as sponsor contact, oversee team members, assist in hiring and training

Seniority

Mid-Senior, hands-on IC with leadership duties

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