Associate, Study Management III

📋 Description

• Lead and contribute to global clinical trials from inception through closure
• Provide study-level oversight in a cross-functional global environment
• Support strategic leadership, stakeholder engagement, and timely documentation
• Manage vendors, recruitment, and study materials ensuring quality and timelines
• Lead meetings, prepare updates, and ensure inspection readiness
• Collaborate on CTMS/eTMF/EDC/IRT/ePRO systems and study deliverables

🎯 Requirements

• Bachelor’s Degree or equivalent required
• 4+ years Pharma/clinical research experience
• Familiar with SOPs, ICH/GCP, and global regulations
• Experience with EDC, IRT, CTMS, and eTMF systems
• Strong analytical, organizational, and global communication skills
• Independent, proactive, collaborative, and able to work in a fast-paced global team

🎁 Benefits

• AbbVie equal opportunity employer
• Comprehensive benefits package; eligibility for short-term incentive programs
• Global exposure and opportunity for career development