Study Coordinator / Study Nurse / Studienassistent:in (a)

As a traditional, leading university hospital, Inselspital is a medical competence and high-tech center with international appeal and at the same time a place of education and research of the first rank. The mission of the RND study team is to advance knowledge in the field of rare neurodegenerative diseases by promoting high-quality, innovative, and effective research. Our vision is to significantly improve the care of patients with RNDs. What to expect <br /> • Independent project management of clinical studies in the hospital as an interface to sponsors and CRO • GCP-compliant implementation of the study • Care of study participants • Planning, coordination, implementation, and documentation of patient visits (including infusions, blood sampling, sample processing in the laboratory, vital signs, patient scores, questionnaires, EKG recording, etc.) • Completion of the case report form (CRF), entry of data into electronic databases (eCRF) as well as maintenance and quality control of databases (queries, corrections, etc.) • Preparation and support of monitoring visits (on-site monitoring, remote monitoring) • Correspondence with internal and external partners (e.g., sponsor, monitors, laboratory) • Maintenance of study-relevant documents (Investigator Site File, Delegation Log, Training Log, etc.) • Collaboration in compliance with regulatory requirements (SOPs, SAE reports, etc.) <br /> What you bring <br /> • Dipl. Pflegefachperson HF/FH (or equivalent), preferably with experience in the pediatric environment • CAS Clinical Research Coordinator or several years of experience as a Study Nurse • Thorough, organized, and independent work style with high initiative • Empathetic and responsible interaction with patients • Team-oriented, reliable personality with a lot of commitment • Very good German language skills as well as good knowledge of English and French <br /> Our offer <br /> • Varied and challenging activity with high practical relevance and tangible added value for those affected • Collaboration in a collegial and motivated team • Opportunity for professional and personal development, including further qualifications and sharpening of one's own profile • Flexible working hours possible after consultation <br /> Questions about the position? Further information is provided by Sandrina Schneider Clinical Research Manager +41 31 632 07 41