Description

With more than and representing 160 professions, the Geneva University Hospitals are a reference institution at the level and To learn more about our institution, take a few minutes to consult our retrospective by clicking here. Counting more than the Department of fulfills a triple mission focusing on the treatment of psychic disorders, and the Department of conducts innovative research, covering a wide spectrum of approaches, notably clinical trials in psychotherapy, in and in pharmacology. It also develops mechanistic studies anchored in neurosciences and integrating multimodal approaches. Furthermore, the department conducts research focused on care and the Clinical Research Center (CRC) of the Geneva University Hospitals (HUG) and its multidisciplinary team support researchers in all stages of their research projects or scientific - 80% This position is in the Department of and is part of a close collaboration with the Clinical Research Center (CRC). You play a key role in clinical research, specializing in regulatory submissions and the of clinical studies. You ensure that all activities are compliant with the as a or you manage clinical studies from phase I to IV as well as studies You communicate regularly with sponsors, the main of the different sites and the CROs involved. You are responsible for document management (ISF/TMF), screening, inclusion and follow-up of participants, data entry, drafting annual safety reports, and you provide support during monitoring, audit and expertise visits allows you to handle submission requests and regulatory affairs for clinical studies, including drafting the protocol, consents and study documents. In with the you coordinate clinical research projects from institutions and the pharmaceutical industry, thus guaranteeing rigorous compliance with the laws, regulations and guidelines necessary for research of You are in possession of at least a Bachelor's degree in the scientific field. In addition, you benefit from complementary training in clinical research, such as a Diploma X Studies-DAS, continuing education in Management of Clinical Trials, that Inter-University (DIU) of to clinical trials of drugs (FIEC) or a deemed equivalent. You justify at least five years of experience in the field of clinical research and possess excellent knowledge of the Swiss and more, you perfectly master French and English both orally and in writing. You possess very good you know how to demonstrate autonomy and work within the framework of a team. Additional information Start date: Number of positions: 1 Activity rate: 80% Function class: : Fixed-term contract 1 year Deadline for: Request for information: Dr. deputy physician unit manager, tel, Write an email Mr. deputy physician unit manager, tel, Write an email Your application file must include a letter demonstrating your your curriculum vitae, copies of diplomas and required for the position and the last 2 of This advertisement is addressed indiscriminately to women and men. Wishing to commit to the fight against unemployment, the HUG encourage those who come from the cantonal office of the those submitted via the recruitment platform are taken into account. Paper and email applications will not be processed. jid38c0a48aen jit0832aen jpiy26aen