Study Nurse Gastroenterologie/Hepatologie 80%

Descrizione del posto

Clarunis Universitäres Bauchzentrum Basel is a specialized center for abdominal treatments. Join a collaborative environment focused on improving patient care and outcomes. Tasks Coordinate visits with study teams following GCP guidelines. Manage, prepare, and return various study materials efficiently. Document study data and report any adverse events accurately. Skills Experience in clinical studies and adherence to ethical standards required. Strong communication and organizational skills essential. Proficiency in data management and regulatory compliance needed. This job ad was AI-translated from German. See original About the job Clarunis University Abdominal Centre Basel is the joint competence centre of Claraspital and the University Hospital Basel for all patients requiring treatment in the abdominal area. Clarunis combines the expertise, research activities and number of patients treated at both hospitals to further enhance and improve the quality of diagnosis and treatment. The Study Nurse is responsible for the quality-compliant support in the planning, implementation and documentation of clinical studies. They ensure compliance with legal and ethical requirements as well as internal guidelines and contribute significantly through their professional conduct to ensuring a smooth study process. Study Nurse Gastroenterology/Hepatology 80% Your tasks include: Coordination of visits in close collaboration with study teams according to GCP guidelines Registration, randomisation and allocation of study medication Preparation, management, maintenance and return of various study materials Collection, processing and shipment of blood samples according to IATA guidelines Co-management of study medication according to the requirements of study protocols Support in conducting monitoring visits Communication with study participants and scheduling of study visits Support of medical staff in screening and inclusion of study participants as well as obtaining informed consent Collection and documentation of study data in medical records, source documents and case report forms (CRF) with data entry Recording and reporting of adverse events (AE / SAE) Updating and archiving of study documents Collaborative projects with the Department of Biomedicine (DBM) and Department of Clinical Research (DKF) of Basel We offer: a lively and collegial working environment with supportive colleagues interesting opportunities for further training attractive employment conditions with generous social benefits good accessibility of the workplace (train, tram, bus, bicycle) If you feel addressed and are ready to take on this challenge, we look forward to receiving your online application.