IrvineFull TimeOperations
Remotely
gcpproject managementregulatory compliancementoringich guidelinesclinical data strategycdso
Also available on
Job Description
📋 Description
- Aligns CDSO study teams with program- and study-level strategies and governs assigned programs and
- Acts as operational lead from CDSO; coordinates study teams to meet objectives.
- Engages global functional and cross-functional teams at program and study levels.
- Uses operational analytics and project management tools to optimize execution and track progress.
- Ensures adherence to GCP, ICH Guidelines, AbbVie SOPs and regulatory standards.
- Coaches and mentors team members and leads cross-functional improvements.
🎯 Requirements
- Bachelor’s degree in business, MIS, CS, life sciences or equivalent. Master’s preferred. PMP or
- 8+ years pharma/clinical research/data management or 10+ years project management.
- Deep understanding of clinical trial processes and stakeholder management.
- Proven cross-functional leadership, influence without authority, and strong
🎁 Benefits
- We offer a comprehensive benefits package including PTO and medical/dental/vision insurance.
- Eligible to participate in short-term incentive programs.
- Equal Opportunity Employer/Veterans/Disabled.