Coordonnateur/coordonnatrice de recherche clinique

Coordinate clinical trial activities from launch to closure by preparing and submitting regulatory documents, maintaining accurate trial records, and coordinating meetings with minutes generation. Support the clinical team through project reporting, scheduling, and logistics while managing communications with clinical centers and vendors. Ensure compliance with regulatory requirements and Good Clinical Practices by verifying ethical committee activities, payment tasks, and site activation checklists. Assist with drafting confidentiality agreements, clinical center contracts, and budgets. Collaborate on site activation documents and payment tracking to ensure medication release accuracy.