Beschreibung

- Quality monitoring, clinical and scientific research - 60%With more than 160 professions, the Geneva University Hospitals are a reference institution. To learn more about our institution, take a few minutes to consult our retrospective.The Urology Service of the Surgery Department of the HUG ensures the diagnosis and treatment of patients suffering from an affection of the organs of the urogenital system (kidney, bladder, prostate). It is recognized as a center of excellence in terms of surgical expertise, particularly for the treatment of prostate cancer, thanks to the quality label issued by the European Cancer Centers (ECC).It offers patients care of the highest level in close collaboration with other specialties: anesthesia, nephrology, radiology, oncology, radiation oncology, visceral surgery, etc.In addition to its hospital activities, the service also ensures an academic activity of research and teaching, jointly with the Faculty of Medicine.- Quality monitoring, clinical and scientific research - 60%You coordinate the monitoring, the management and the evolution of databases related to quality control, and to the clinical research activities of the service by guaranteeing the coherence, the exploitability and the update of clinical data.You work transversally with the Cancer Center of the institution and the quality manager (QMS), for the monitoring and the preparation of ECC (European Cancer Center) audits.You actively participate in the management, in the implementation of research projects and studies in progress in the service.You collaborate closely with doctors as well as with internal and external stakeholders, by providing methodological support.You participate in the design of studies, in the development of protocols, and in research projects initiated by the investigators (IIT – Investigator Initiated Trials).You ensure the smooth running of studies according to research protocols and in compliance with Good Clinical Practices (ICH-GCP) and regulatory requirements.You contribute to the management of studies (TMF/eTMF), to the quality of data, as well as to monitoring activities, and to the preparation for audits and inspections.You ensure the management of exchanges with ethics committees and Swiss regulatory authorities (Swissmedic) and in connection with the sponsors and partners concerned.You ensure a liaison role between clinical teams, researchers and external partners.You participate in the analysis and processing of data, in the creation of scientific supports (graphs, figures, diagrams, etc.) and in the drafting of study documents (eCRF, forms, etc.) and in the coordination of the service's activities.You hold a Bachelor's degree in a field relevant to clinical research and a CAS in clinical research.You benefit from 5 years of experience in clinical research, managing projects in a medical environment.You have excellent knowledge of Good Clinical Practices (ICH-GCP) and the regulatory environment.You master current office tools, clinical databases; experience with EDC/REDCAP/eTMF/Adjumed appreciated.You possess project management skills, with a strong capacity for adaptability and organization.You are able to produce scientific supports and you also have writing skills.You are able to work autonomously, with rigor, reliably, with a keen sense of responsibility, and to manage several priorities effectively in a medical and scientific environment.You identify effective solutions and you have a marked interest in clinical research and oncology.You have very good English skills, both oral and written.This position is subject to a specific schedule in coordination with other clinical or scientific staff to ensure the proper functioning of the service during working days.Position details:Number of positions: 1Activity rate: 60% (+20% the 1st year, renewable)Job class: 14Contract type: Permanent contractApplication deadline: [Date removed]Permanent contract based on 60%. Ideally, during the 1st year, activity rate desired at 80% (renewable possibly for the 2nd year).Your application file must include a letter demonstrating your motivation, your curriculum vitae, copies of diplomas and certificates required for the position and the last 2 performance reviews.This announcement is addressed indiscriminately to women and men.Wishing to commit to the fight against unemployment, the HUG encourage candidates who come from the cantonal employment office to apply.Only applications submitted via the recruitment platform are taken into account. Paper and email applications will not be processed. jid58d70e4aen jit0416aen jpiy26aen