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Clinical Research Nurse I

Lodzi, Poland💼 Full-time🗓 2026-04-27 → 2026-09-26

Core

Conduct clinical trials involving patients or healthy volunteers, ensuring subject safety, data capture, and study protocol adherence.

Role type

Clinical Research Nurse (IC)

Builds

Clinical trial data and patient care services for global health research

Domain

Clinical research / Life sciences

Deliverable

physical/clinical work

Required skills

Clinical trial execution, patient care, data recording, regulatory compliance (FDA/GCP/ICH), recruitment and retention, informed consent, vital signs monitoring, IRB coordination

Preferred skills

English fluency, computer proficiency, independent work, problem solving

Technologies

EDC systems, case report forms, office software

Responsibilities

Conduct clinical studies per FDA/GCP/ICH guidelines; provide medical care to patients; schedule subject visits; perform study activities (screening, vital signs, ECGs); record patient data and test results; manage patient recruitment and retention; ensure IRB approval and compliance; maintain source documents and patient files; report non-compliance; attend site meetings for training.

Seniority

Mid-level, hands-on IC

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