CareerPlan

Study Nurse / Dokumentationsassistenz (m/w/d) für Hämatologie und Onkologie

Cottbus, BRANDENBURGFull-time2026-06-19 → 2026-11-10
Hybrid

Core

Coordinate clinical trials in hematology and oncology, managing patient care, data documentation, and study logistics.

Role type

Study Nurse / Clinical Research Coordinator

Builds

Clinical trial data and patient care processes for hematology and oncology research

Domain

Healthcare / Clinical Research

Required skills

Patient care, GCP compliance, Adverse Event reporting, Medication management, SOP development, Study coordination

Preferred skills

Study Assistant certification, GCP certification, MS Office proficiency

Technologies

MS Office, Electronic Data Capture systems (implied by documentation systems)

Responsibilities

Coordinate communication between investigators and sponsors, manage study patient care and diagnostics, maintain GCP-compliant documentation, organize study logistics and medication handling, develop study-specific SOPs, oversee administrative study organization

Seniority

Mid-level, hands-on IC