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Program Manager, Clinical Supplies Management
AbbVie. Serve as manager of Clinical Supply Project Managers (CSPMs), or provide individual-contributor oversight of key pipeline studies across multiple CSPMs .
Posted 11/3/2026full-timeRemote • Illinois • United StatesMid-LevelSenior💰 $124,500 - $236,500 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates extensive experience in Clinical Supplies Project Management, with a strong focus on developing compliant processes and monitoring project quality. Proven ability to lead cross-functional initiatives and evaluate issues from a global perspective.
Highest-signal resume keywords
Clinical Supplies Project ManagementProcess DevelopmentQuality MonitoringCross-Functional CollaborationGlobal Perspective
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Project ManagementProcess ComplianceIssue EvaluationAgility ImprovementCost-Effective Study Management
Soft Skills
LeadershipProblem SolvingCommunication
Industry Keywords
Clinical TrialsR&D ComplianceScientific DisciplineGlobal Operations
About the role
Key responsibilities & impact- Serve as manager of Clinical Supply Project Managers (CSPMs), or provide individual-contributor oversight of key pipeline studies across multiple CSPMs
- Monitor the effectiveness of processes and quality of CSPM project work
- Work globally and cross-functionally to ensure cost-effective study management and high-quality outcomes
- Lead development of new processes to ensure compliance in Clinical Supplies Project Management
- Work on large cross-functional improvement initiatives to increase agility and compliance across AbbVie R&D
- Evaluate issues and propose solutions with a global perspective
- Represent Clinical Supplies Project Management
Requirements
What you’ll need- BS or equivalent education and typically 14+ years of experience in the area or scientific area of discipline
- MS or equivalent education and typically 12+ years of experience in the area or scientific area of discipline
- PhD and typically 6+ years of experience in the area or scientific area of discipline
- Experience in clinical supplies project management
- Ability to monitor processes and quality of project work
- Ability to work globally and cross-functionally
- Ability to develop compliant processes
- Ability to evaluate issues and propose solutions with a global perspective
Benefits
Comp & perks- Paid time off (vacation, holidays, sick)
- Medical, dental, and vision insurance
- 401(k)
- Eligibility to participate in long-term incentive programs