Your impact
You will contribute directly to the quality and integrity of clinical trial data in a technology-driven imaging environment. Your work ensures that study results are complete, consistent, and audit-ready.
Your responsibilities
- Own and maintain the query log: identify, track, and resolve data inconsistencies, missing information, and quality issues
- Continuously review and validate study results (completeness, consistency, plausibility)
- Support the structuring and optimization of study processes and contribute to our tech platform
- Assist Study Coordinators in day-to-day project work across multiple clinical studies
- Collaborate cross-functionally with Data Management, Study Coordination, and IT
Your profile
- Enrolled student (Life Sciences, Medicine, Biomedical Engineering, Data Science, or similar)
- Experience working with structured data (Excel or similar tools)
- Strong analytical mindset with high attention to detail
- Independent, structured, and reliable working style
- Good communication skills and ability to work in a team
- Fluent English (mandatory); German is a plus
What we offer
- Flexible working hours aligned with your studies
- Hybrid setup: work remotely or from our office in Hamburg (Hoheluft)
- Direct involvement in international clinical trials
- Opportunity to actively shape processes in a medical deep-tech company
- Close collaboration with leading experts in neuroradiology
Why this role matters
High-quality data is the foundation for clinical decisions and regulatory submissions. Your work directly contributes to reliable outcomes and real-world impact.
Apply with CV and short motivation.