Study Nurse (m/f/d)

Communication and support of test physicians in administrative and organisational processes in clinical trials Study Coordination (Clinical Studies Phase II-IV, Non- Interventional Studies (NIS)) Care of study patients according to study protocol, administering test medication Collection, collection and documentation of the study-specific data from patient records, leaflets, investigation logs Quality assurance acceptance and processing of blood samples, sample delivery Project submission to Ethics Commission and Authorities Coordination and assistance in studies Preparation of monitor visits, support of monitors with regard to data monitoring and compliance with the study schedule Communication with study societies, study groups, sponsors, monitors, the medical chamber, the doctors Computer activity with data management, creating files, tables Creating PowerPoint slides

Complete training for medical professionals or for health and safety Nurse, ideally with qualification for the Study Nurse or with willingness to acquire this qualification At least 1 year experience in the planning, implementation and coordination of clinical studies Knowledge in the field of mamma and/or ovarian carcinoma would be desirable Self-functioning, reliability and flexibility Teamability, contactability and sensitivity for tumor patients Good computer skills Very good English skills in word and writing

Implementation of own ideas and work in an innovative interdisciplinary team Agreement of flexible working hours to translate the connection of family and profession into reality Participation in vocational training, training and training opportunities Compensation with the associated social benefits according to the rate of the diaconic work