Universitätsklinikum Köln (AöR) | Germany | 50xxx, 51xxx Köln | Temporary contract | Part time - flexible / Full time | Published since: 25.08.2026 on stepstone.de
Project Assistant / Study Assistant Internal Medicine - GHSG-Studienzentrale (m/f/d)
Your future with us We are one of the leading university clinics in Germany and network research, teaching and health care at top level. That's why we have a number bigger: the spectrum of exciting development possibilities. The limitless openness with which specialists from all over the world work together. Or our commitment as an employer, all employees so well we can help to reconcile the profession with their goals and situations of life. This is the University Hospital Cologne: Everything, except usual. To support our growing team, we are looking for the next time: Projektassistance (m/d) Internal Medicine – GHSG Study Centre The German Hodgkin Study Group (GHSG) under the leadership of Professor Peter Borchmann is the world's leading research group in the field of Hodgkin lymphoma. The results of the multicentric clinical studies have been contributing significantly to the continuous improvement of the forecast of patients with Hodgkin lymphoma for 40 years. The GHSG is a member of the Maligne Lymphome competence network. As a study center of the GHSG (Head of Mr. Michael Fuchs), we are organizationally assigned to the Klinik I for Internal Medicine of the University of Cologne. Our tasks are planning, preparation, organisation, implementation and evaluation of the GHSG studies and systematic analyses using our study database with over 20,000 patients. In our team, various areas such as medicine, statistics, data management, project and quality management and programming work closely together. The project assistance area supports project management. 38.5 hours/week Deadline for 1 year Remuneration takes place according to TV-L to EG 6
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Your tasks • Your profile • What we offer
Support of the project manager in the field of clinical trials of phases I to III Design and creation of study folders such as Trial Master File (TMF), Investigator Site File (ISF) and patient folders Application, collection, review and provision of study documents for submissions or for filing in the TMF / ISF Management of TMFs, including maintenance of overview tables to ensure the completeness of the TMF Preparation of the regulatory release of the test medication (sponsor release) Management of study-specific training documentation of the study team and review for completeness ISFs, laboratory kits or other study materials and documents Contact and address management in the database Application, detection, verification and prosecution of final documents at the end of the study and the archiving of TMFs
Training in a scientific, pharmaceutical or medical field (e.g. nursing, MTA, PTA etc.) or as a medical/doc Ideally first experience in conducting clinical trials Experience in handling computer software (especially Word, Excel, Outlook, PowerPoint, electronic data acquisition) Good knowledge of English
Everything, except usual: You expect a safe and meaningful job in a challenging working environment where you are always at the heart of time. Job and private life in line with: Thanks to the flexible working time account and desired service plans, you have more time for hobbies, family and friends. Team spirit in R(h)einkultur: You will be welcomed by an interdisciplinary team with open arms that will increase mutual appreciation and helpfulness. Strong perspectives: What other people gain experience across different stations is one of the largest employers in the region under one roof – so you can grow beyond yourself and target new goals. .
Location
 | Universitätsklinikum Köln (AöR) | |
| 50937 Köln | ||
| Germany |
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