North AmericaFull TimeOperations
Remotely
ctmsedcetmfeproirt
Job Description
📋 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
