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. #J-18808-Ljbffr