Study coordinator 80 - 100 %
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Description du poste
### The University of Zurich, Switzerland's largest university, offers a range of attractive positions in various subject areas and professional fields. With around 10,000 employees and currently 12 professional apprenticeship streams the University offers an inspiring working environment on cutting-edge research and top-class education. Put your talent and skills to work with us. Find out more about UZH as an employer! ### Your responsibilities **Support Scientific Project Work within CEREBRIS:** * Support acquisition and analysis of multimodal data (EEG, fNIRS, MRI, CT, motion capture, clinical scores) * Support development and validation of neurophysiological markers in alignment with imaging-derived biomarkers * Support conducting bias and fairness analyses for AI-based biomarkers * Support contributing to the development of clinically deployable AI by benchmarking against validation frameworks * Support the implementation of ISO 9241-210-conformant usability studies (dashboards, ePRO/eCRF) **Clinical Trial Coordination and Data Management:** * Recruitment and clinical management of stroke patients * Obtaining informed consent (German required, swiss german is an advantage) * REDCap database management * Study logistics, SOP implementation, monitoring support * Ensuring data quality and regulatory compliance * Main contact point for clinical trial center **Support Scientific Publication and Dissemination:** * Support publishing in high-impact international journals * Support presenting at national and international conferences * Support preparing reports for project partners and funding agencies **Support Health Technology Assessment & Translation:** * Contributing to early-HTA micro-scenarios * Supporting development of modelling cost-benefit scenarios within the Swiss healthcare system * Supporting payer and stakeholder briefings Your profile * Completed Master's degree (MSc) in Biomedicine, Neuroscience, Biomedical Engineering, Psychology, Data Science, Physio-or Occupational Therapy or related field, Solid knowledge of trial management, knowledge of statistics and study design, basic experience in Python, and strong knowledge with REDCap or comparable systems; knowledge of clinical workflows and processes * Experience in conducting clinical trials and patient recruitment mandatory, basic knowledge of neuroimaging or motion capture is an advantage * Professional Responsibility: Independent planning and execution of defined study modules, Responsibility for data integrity, support development of methodological standards for translational AI in stroke, Financial Responsibility: No budget responsibility, Ressource planning within allocated project funding; Collaboration: Close cooperation with Postdoc, project leadership, and international consortium partners; Collaboration with neurology, radiology, and neurophysiology departments; Interaction with data scientists and industry partners Reporting Duties:Regular reporting to project leadership Documentation according to GCP standards Christoph Bauer PostDoc Christoph.bauer@uzh.ch
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