CareerPlan

Studienassistenz (Study Nurse) / Studienkoordinator:in (all genders) für das onkologische...

Hamburg, HAMBURGFull-time€43k2026-10-06 → 2026-11-03

Core

Coordinating and supporting oncology clinical trials for new cancer therapies within a multidisciplinary team.

Role type

Clinical research coordinator / study nurse

Builds

Clinical trials for oncology therapies

Domain

Healthcare / Oncology / Clinical Research

Required skills

Clinical nursing background, GCP knowledge, data management, protocol compliance, patient care, documentation, study logistics

Preferred skills

Prior clinical research experience, bilingual German/English, advanced MS Office, certification in study assistance

Technologies

MS Office, Electronic Data Capture systems (implied by data entry)

Responsibilities

Coordinate clinical studies from initiation to completion, submit studies to authorities and ethics committees, design data collection forms, organize study visits and sample collection, manage patient data and documentation, support monitor visits and audits, train study team members

Seniority

Entry to Mid-level, structured onboarding available