Clinical Trial Assistant

What you'll do:

• Collaborate with the team to plan, coordinate, and execute clinical research studies.
• Craft, maintain, and archive essential documents for regulatory compliance and smooth study execution.
• Assist in preparing key documents for regulatory submissions.
• Maintain open communication with clinical trial sites (domestic and international) to ensure successful study conduct.
• Handle general administrative tasks like organizing meetings, creating presentations, and taking minutes.

Who you are:

• You hold a degree in a relevant field (medicine, science, or business) and ideally have experience in clinical research.
• A meticulous and organized individual with a strong work ethic and a knack for structure.
• A true team player with a go-getter attitude and initiative.
• Excellent communication skills and a natural ability to connect with others.
• Proficient in MS Office Suite (Word, Excel, PowerPoint).
• Fluent in German (C1 level minimum) and possess strong English skills (B2 level minimum).

What we offer:

• A dynamic and challenging role with exciting tasks and opportunities to make a mark.
• An innovative environment that fosters career growth with clear decision-making channels and the freedom to explore new approaches.
• A collaborative work culture with flat hierarchies and open communication.
• The chance to take ownership after an onboarding phase with a dedicated mentor.
• Flexible work arrangements – a healthy balance between on-site and remote work.
• Weekly fruit basket to keep you energized!
• Fun company events like summer parties, Oktoberfest visits, and holiday celebrations.
• A rooftop terrace with stunning alpine views for relaxing breaks.