Description
IQVIA, a world-leading organisation in clinical research and healthcare, is seeking a dedicated Study Nurse / Study Coordinator to support a clinical study at its Kempten site.
This part-time position (24 hours per week) is available immediately and is initially contract-based for 6 months.
Your Responsibilities
- Coordinate and organise study-related processes on-site
- Provide care and support to study participants during the study implementation
- Manage and maintain study data in electronic data capture systems (EDC)
- Ensure high data quality and completeness of study documentation
- Assist with patient screenings, appointment planning, and recruitment measures
- Organise logistical study processes according to the study protocol
- Collaborate closely with investigators, monitors, and other study stakeholders
- Adhere to GCP guidelines and study-specific requirements
Your Profile
- Experience in clinical research
- Familiarity with electronic data capture systems (EDC Data Management)
- Experience in patient management and study participant care
- Two years of relevant professional experience in clinical trials or a comparable combination of education and practical experience
- Good knowledge of study-specific processes, study documentation, informed consent procedures, and study protocols
- Proficient in MS Office applications (Word, Excel, Outlook)
- Excellent organisational skills and attention to detail
- Strong communication skills and ability to work with patients and interdisciplinary teams
- Fluency in German (written and spoken)
What We Offer
- Opportunity to work on an innovative clinical study with a world-leading research organisation
- Varied tasks with direct patient contact
- Flexible part-time employment with 24 hours per week
- Professional and supportive team environment
- Chance to further develop your expertise in clinical research and gain valuable project experience