• Develop study protocols in collaboration with clinical, statistical, and regulatory teams
• Take full ownership of trial operations – from start-up to publication
• Coordinate external partners including CROs, trial sites, and technical vendors across Germany, Switzerland, and the UK
• Oversee budgets, timelines, milestones, and risk management
• Share your expertise to foster a collaborative, learning-oriented team culture
• Ensure data quality, regulatory compliance, and audit readiness at all times

Our requirements

• A degree in life sciences, medicine, or a related field
• Proven experience in protocol development, statistics, literature review, and clinical trial execution
• In-depth knowledge of ICH-GCP, ISO14155, EU MDR, and local regulatory environments in DE, CH, and UK
• Hands‑on experience with CTMS, EDC, eTMF, IWRS/eCOA, and user acceptance testing
• Strong communication skills, a problem‑solving mindset, and collaborative spirit
• Fluent in English (spoken and written) – German is a plus!

What we offer

• A meaningful role where your work drives real impact in healthcare
• A dynamic and purpose‑driven environment in a fast‑growing organisation
• Extensive training and development opportunities, including a personal learning budget
• Flexible working models and remote‑first options to support your work‑life balance
• A home office allowance to help you create your ideal workspace
• Competitive salary and company pension scheme