Study Nurse (m/w/d) / Studienkoordinator:in | 24 Std./Woche | Kempten
IQVIA · Bayern, Germany
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Role summary
A clinical research organization seeks a part-time Study Nurse and Study Coordinator (24 hours/week) for a clinical trial in Kempten. The role involves coordinating study activities, managing participant care, maintaining electronic data systems, and ensuring compliance with GCP guidelines. The position is fixed-term for six months, requiring two years of clinical research experience and proficiency with EDC systems.
What they're looking for
- Clinical research experience with study protocols and documentation
- Proficiency with electronic data capture systems for study management
- Patient management and study participant care experience
- Two years relevant clinical trial work or equivalent education/experience combination
- Knowledge of GCP guidelines and informed consent procedures
- Microsoft Office proficiency and strong organizational skills
- Fluent German language skills in writing and speaking
What you'll be doing
- Coordinate and organize all study-related processes at the Kempten site
- Manage study participant recruitment, screening, and appointment scheduling
- Maintain study data quality and completeness in electronic systems
- Collaborate with principal investigators, monitors, and study team members
- Ensure compliance with GCP guidelines and study protocol requirements
Privacy & handoff
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