Clinical Project Manager

Role: Lead and manage cross-functional clinical study teams and CROs to ensure effective study execution in line with quality, timelines, and budgets. Responsibilities: oversee study team communication; coordinate study activities from startup to CSR; develop project plans, budgets, and oversee vendor selection and relationships; ensure regulatory compliance and data integrity; support patient recruitment strategies and site selection; collaborate with internal departments (Regulatory, Pharmacovigilance, Data Management) and external vendors; contribute to SOP updates and transversal projects; participate in audits and inspections; and contribute to clinical reports and registry submissions. Requirements: Bachelor's in life sciences or relevant qualification; minimum 3 years in clinical research, with 2+ years managing international registrational studies; experience working with CROs, multidisciplinary teams, and in regulated environments; fluency in English; strong organizational, leadership, and communication skills; knowledge of GCP, ICH E6, EU directives, and pharmaceutical R&D processes. Preferred: experience in drug development, budget management, and working within QMS. High-Value: experience managing global clinical trials, particularly in regulated pharmaceutical environments, with responsibilities spanning study setup, vendor oversight, regulatory compliance, and cross-functional coordination. Work setup: not specified; travel may be required.