Studienkoordinator:in / Clinical Research Coordinator / Study Nurse (m/w/d)
IQVIA · Thuringia, Germany
Clinical OperationsPart-timeCompany career page
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Role summary
IQVIA seeks an experienced clinical research coordinator or study nurse for a part-time role (20 hours/week) at a study site in Erfurt. The position involves coordinating an ongoing clinical trial, managing patient care, conducting study visits, and maintaining study documentation for approximately six months.
What they're looking for
- Minimum 2 years clinical research experience (Study Nurse, CRC, or Coordinator)
- Strong knowledge of data and visit management in clinical trials
- Proficiency with EDC systems
- Fluent German (written and verbal)
- Proficient with MS Office and general IT skills
- Organized, reliable, and patient-focused work approach
What you'll be doing
- Coordinate and manage clinical study under Principal Investigator delegation
- Schedule, conduct, and document study visits with participants
- Enter, verify, and manage study data in EDC systems and case report forms
- Support participant recruitment, screening, and enrollment processes
- Liaise with monitors and respond to study-related inquiries
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.