Clinical Research

• 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

Explore Senior Clinical Trial Manager at AbbVie. Review requirements and application details.

Senior Clinical Trial Manager

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