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

Job Data by YubHub.