Study Project Manager I

The Study Project Manager I drives the connection between science and operational delivery and ensures operational excellence in planning and execution of clinical research studies across all development stages.

Requirements

• Defines and drives the operational strategies and deliverables for one or more clinical studies
• Responsible for executing clinical studies in compliance with quality standards (ICH/GCP, Global Regulations, and AbbVie policies and procedures).
• Proactively manages budget, timelines and study issues; brings scientific acumen, technical expertise and global mindset to drive achievement of study objectives
• Effectively manages vendors and a diverse set of external stakeholders including site staff, Key Opinion Leaders and patient groups
• Coaches and effectively supports cross functional team members, delegates and empowers to the right level, actively contributes to Development Operations community
• Contributes towards operational efficiencies and brings innovative ideas to their teams and studies
• Demonstrates excellent communication and problem solving skills
• Puts patients and customers at the center of what we do
• Navigates ambiguity and thrives even when not having all the information