Scientific Collaborator - 80%

With more than 13'000 employees representing 160 professions, the Hôpitaux Universitaires de Genève are a leading institution at national and international levels. To learn more about our institution, take a few minutes to consult our 2025 retrospective by clicking here. With more than 1'300 employees, the Department of Psychiatry responds to a triple mission involving the treatment of mental disorders, training, and research. The Department of Psychiatry conducts innovative translational research, covering a wide spectrum of approaches, including clinical trials in psychotherapy, neuromodulation, and pharmacology. It also develops mechanistic studies anchored in neuroscience and integrating multimodal approaches. Furthermore, the department conducts research focused on improving psychiatric care and clinical practices. The Centre de Recherche Clinique (CRC) of the Hôpitaux Universitaires de Genève (HUG) and its multidisciplinary team support researchers at all stages of their clinical research projects. Scientific Collaborator - 80% This position is attached to the Department of Psychiatry and is part of a close collaboration with the Centre de Recherche Clinique (CRC). You play a key role in clinical research, specializing in regulatory submissions and the coordination of clinical studies. You ensure that all activities comply with current regulations. As a coordinator, you manage phase I to IV clinical studies as well as observational studies. You communicate regularly with sponsors, principal investigators from different sites, and the involved CROs. You are responsible for document management (ISF/TMF), screening, inclusion, and follow-up of participants, data entry, writing annual safety reports, and you provide support during monitoring visits, audits, and inspections. Your expertise allows you to handle submission requests and regulatory affairs for clinical studies, including the drafting of protocols, consents, and study documents. In collaboration with investigators, you coordinate clinical research projects from institutions and the pharmaceutical industry, thus guaranteeing rigorous compliance with the laws, regulations, and guidelines necessary for quality research. Qualifications You possess at least a Bachelor's degree in a scientific field. Furthermore, you benefit from additional training in clinical research, such as a Diploma of Advanced Studies-DAS, continuing education in "Management of Clinical Trials", an Inter Universitaire (DIU) "Formation des investigateurs aux essais cliniques des médicaments (FIEC)", or training deemed equivalent. You have at least five years of experience in the field of clinical research and possess excellent knowledge of Swiss and international regulations. Additionally, you have perfect mastery of French and English, both oral and written. You possess very good communication skills, know how to demonstrate autonomy, and work within a multidisciplinary team. Additional information Start date: Number of positions: 1 Activity rate: 80% Function class: 17 Contract: 1 year fixed-term contract Application deadline: Inquiry: Dre D.Alfaiate, médecin-adjointe responsable d'unité, tél , Write an email (< >) M.Kirschner, médecin-adjoint responsable d'unité, tél , 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 advertisement is addressed indistinctly 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 will be considered. Paper and email applications will not be processed. jpid38c0a48jm jpit0832jm jpiy26jm