Study Nurse (m/w/d) / Studienkoordinator:in | 24 Std./Woche | Bochum
IQVIA · Bochum, Germany
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Role summary
This part-time study nurse and coordinator role (24 hours/week) supports a clinical trial in Bochum from October 2026 through March 2027. Responsibilities include managing study participants, maintaining data quality in electronic systems, coordinating logistics, and ensuring GCP compliance. Candidates should have at least two years of clinical research experience, EDC proficiency, and strong organizational skills.
What they're looking for
- Two years of relevant experience in clinical trials or equivalent education and practical experience
- Experience with electronic data capture systems and EDC data management
- Knowledge of study protocols, documentation, informed consent procedures
- Proficiency in MS Office applications (Word, Excel, Outlook)
- Strong organizational skills and attention to detail
- Fluent German language skills, written and spoken
- Communication abilities and experience collaborating with interdisciplinary teams
What you'll be doing
- Coordinate and organize all study-related processes at the Bochum site
- Manage study participant recruitment, screening, scheduling, and support throughout the trial
- Maintain study data in electronic data capture systems and ensure data quality and documentation completeness
- Support logistical study processes according to study protocol and collaborate with investigators and monitors
- Ensure compliance with GCP guidelines and study-specific requirements
Privacy & handoff
This role links to IQVIA's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.