Attaché(e) de Recherche Clinique (ARC)

• Ensure quality and regulatory compliance of clinical trials on Bundibugyo virus Ebola in the Democratic Republic of Congo, adhering to ICH-GCP guidelines and supporting MSF's humanitarian objectives
• Lead the development and implementation of risk-based clinical monitoring plans across study sites
• Manage clinical monitoring activities, including direct site visits, report writing, and supervision of external monitoring providers
• Coordinate submission of research protocols to local, national and regulatory ethics committees, ensuring complete study documentation
• Drive the quality management system by overseeing investigational product management in collaboration with the responsible pharmacist and operational project teams

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