You hold a Bachelor’s degree preferably in life science or nursing, or equivalent. You bring at least 4 years of on-site monitoring experience in the pharmaceutical/ biotechnology industry (incl. all monitoring visit types), and a comprehensive knowledge of ICH-GCP, FDA and EMA guidelines and applicable local regulations. You have already gained significant insights into clinical trial management activities. Knowledge of basic medical oncology terminology and cell therapy is an advantage.
We expect a high degree of independent working, analytical thinking and excellent communication skills in German and English. You are a good team player and role model with very good organization, negotiation and resolution skills. Travelling up to 30% is acceptable for you. You embrace rapidly changing requirements with an open mind, think outside the box and show a high degree of flexibility in an environment which is marked by a constant striving for excellence. Your motivation is driven by excellence, efficiency and joy at work. You approach tasks in a structured, reliable and foresighted manner, combined with an elevated level of individual responsibility, enthusiasm and strong social skills.