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AbbVie

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 fit
Core Competencies

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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

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Applicant 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