Scientific Collaborator – Coordination of cross-border patient pathways and hospital partnerships - 70%
- Employment type
- Part-time
- Workload
- 70%
- Location
- Genève
- Company
- HUG - Hôpitaux Universitaires de Genève, 1201 Genève
- First posted
Ref 2586568 | Date: 21 Oct 2026 HUG - Hôpitaux Universitaires de Genève With more than 13'000 collaborators representing 160 professions, the Hôpitaux Universitaires de Genève are a reference institution at the national and international level. To learn more about our institution, take a few minutes to consult our 2025 retrospective by clicking [here.](< >) The [Département d'oncologie](< >) provides diagnostic and therapeutic care for adult patients suffering from cancerous diseases and provides support for patients and their relatives. The objective is to ensure access to the best anti-cancer treatment, to propose adapted care, to anticipate the needs of hospitalized patients (bone marrow transplant, cell therapy, immunotherapy, etc.), to strengthen nursing and medical expertise, and to promote research and innovation. The department brings together 4 services (hematology, oncology, precision oncology, and radiation oncology) composed of approximately 300 collaborators with hospital and outpatient activities. Scientific Collaborator -- Coordination of cross-border patient pathways and hospital partnerships - 70% In close collaboration with French and Swiss hospital teams, you provide scientific and methodological support to the project activities. Under the supervision of the project manager, you contribute to the analysis of cross-border patient pathways, the evaluation of new care organizations, the monitoring of scientific activities, as well as the evaluation of digital devices facilitating the identification of patients eligible for clinical trials. You collaborate with French and Swiss hospital teams to collect the information necessary for the implementation of the various phases of the project. As part of the analysis of patient pathways, you participate in the collection and exploitation of information relating to cross-border care pathways. You contribute to the identification of legal, organizational, administrative, and logistical barriers that may hinder access to care and analyze, in collaboration with the French counterpart, the organizational differences between the Swiss and French health systems. Based on these elements, you take part in the drafting of analysis and summary reports and contribute to the development of recommendations aimed at streamlining patient pathways and facilitating access to clinical trials. You also maintain regular exchanges with Swiss and French hospital partners. As part of the pilot project, you participate in the coordination of cross-border patients included in clinical studies. You contribute to the harmonization of administrative and clinical procedures, particularly regarding consents, regulatory documents, insurance, and the organization of patient transport. You participate in identifying the difficulties encountered by patients and health professionals and contribute to the collection of indicators necessary for the evaluation of trial matching tools, as well as the recruitment, identification, and orientation of patients toward clinical trials. Finally, you participate in the interpretation of results and their promotion in the form of technical and scientific reports. Qualifications You hold a Bachelor's degree in a field relevant to clinical research, ideally supplemented by a CAS in clinical research. Thanks to your solid knowledge of good clinical practices and the research environment, you are able to contribute effectively to the conduct and coordination of clinical research projects in collaboration with different partners. You have proven experience in the management or coordination of clinical studies in oncology, acquired in a hospital establishment or in clinical research. Experience within the pharmaceutical industry would be an asset. You are comfortable with the analysis of complex processes and possess a very good knowledge of the regulations applicable to clinical research. Knowledge of the French and Swiss health systems or European projects constitutes an asset Additional information * Start date: to be agreed * Number of positions: 1 * Activity rate: 70% * Function class: 17 * Contract: Private law fixed-term contract * Application deadline: * Request for information: Mme C. Cretton, secretary, [Write an email](< >) Your application file must include a letter demonstrating your motivation, your curriculum vitae, copies of the diplomas and certificates required for the position, and the last 2 work certificates. This announcement is addressed equally to women and men. Wishing to commit to the fight against unemployment, the HUG encourage applications coming from the Office cantonal de l'emploi. Only applications submitted via the recruitment platform are taken into account. Paper and email applications will not be processed. jpid2911a3ejm jpit1043jm jpiy26jm
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Posted 2 weeks ago