Studienassistent/in Klinische Forschung / Dokumentationen

Here's what you'll do:

• Organize, maintain, and archive the TMF, the central filing system for clinical trials.
• Craft and implement plans to keep the TMF running smoothly.
• Become the go-to person for any TMF questions your colleagues have.
• Train new team members on our TMF structure and best practices.
• Conduct regular check-ups on the TMF to identify and address any potential issues.
• Develop and manage tracking tools to monitor the progress of our studies.

We're looking for someone who:

• Has a degree in business, medicine, or science (think office administration or medical documentation).
• Ideally has experience managing clinical trials, especially with TMFs and Investigator Site Files (ISFs).
• Understands the principles of Good Clinical Practice (GCP).
• Is a meticulous organizer with a strong work ethic and a team player spirit.
• Has excellent communication skills in both German and English (C1 level or higher).
• Is a whiz with MS Office (Word, Excel, PowerPoint).

What we offer:

• A challenging and rewarding role where you can make a real impact.
• An innovative environment that encourages professional growth and exploration of new ideas.
• Open communication and flat hierarchies – we value your input!
• The chance to take ownership after an initial training period with a supportive mentor.
• Flexible work arrangements – a healthy balance between working from home and the office.
• Weekly fruit baskets to keep you energized!
• Fun company events to celebrate together.
• A rooftop terrace with stunning alpine views for relaxing breaks.