StudienkoordinatorIn / Study Nurse (m/w/d) - Berlin
IQVIA · Berlin, Germany
Clinical OperationsPart-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
This role coordinates clinical trials in Berlin on a part-time basis (20 hours/week) for approximately six months. The successful candidate will manage patient care, data documentation in electronic systems, and team collaboration while adhering to GCP standards. Candidates should have at least two years of clinical research experience, medical training, and proficiency in German and English.
What they're looking for
- Completed medical training (nursing, MFA, MTA) or life sciences degree
- Minimum 2 years clinical research experience or equivalent qualification
- Proficient with MS Office and EDC systems
- Fluent German (written and spoken); English beneficial
- Strong organizational skills and personal responsibility
- Empathetic patient interaction and teamwork abilities
What you'll be doing
- Coordinate and organize clinical trials according to protocol and GCP guidelines
- Support and accompany study patients throughout trial duration
- Maintain and document study data in CRFs and EDC systems
- Prepare and ship samples; manage study materials
- Collaborate with investigators, monitors, and interdisciplinary teams
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.