Senior Clinical Trial Manager

• Execute one or more elements of clinical studies in compliance with ICH/GCP, Global Regulations, and AbbVie policies and procedures
• Support the Study Project Manager in leading the cross-functional study team
• Support preparation of clinical study team meetings, including agendas and minutes
• Provide regular study-status updates to the cross-functional team and stakeholders
• Keep the CTMS up to date
• Support development of clinical study blueprints, protocols, and associated systems and documents, including informed consent forms, eCRFs, IRT, and CSR
• Support vendor selection, scope development, management, and oversight
• Generate study-related training for study teams, study sites, and vendors
• Proactively identify, resolve, and/or escalate study-related issues
• Participate in process improvement initiatives

• Bachelor’s Degree or OUS equivalent degree, typically in nursing or scientific field
• Registered Nurse licensure with Associate’s Degree in Nursing with relevant experience is also acceptable
• At least four years of pharma-related or clinical research-related experience
• Demonstrated high level of core and technical competencies
• Good communication skills
• Competence in applying standard business procedures, including standard operating procedures, ICH, Global Regulations, Ethics and Compliance
• Preferred exposure to study initiation through study completion
• At least 3 years in clinical trial management positions
• Fluent in English (C1)
• Must be located in Madrid

• Remote work option
• Equal opportunity employment
• Commitment to operating with integrity, driving innovation, transforming lives, and serving the community