Description
The Reference Officer for Clinical Trials and Study Management will independently coordinate the clinical trial portfolio for Clinical Neuro-Oncology, including investigator-initiated and industry-sponsored trials. The role covers methodological design, regulatory and quality management, contract and budget coordination, study-system implementation, and leadership of study nurses, coordinators, project staff, and student assistants. It also involves representing the Study Central Office to sponsors, contract research organizations, authorities, ethics committees, trial sites, and scientific partners. The position is full-time, fixed-term for two years, and requires a relevant scientific degree, several years of clinical-trial or scientific-project experience, GCP knowledge, and strong German and English skills.
