Global Central Monitoring Manager (RBQM)

AbbVie

Florham Park (NJ)

On-site

USD 120,000 - 180,000

Full time

4 days ago
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Benefits offered by this job

Paid time off
401(k)

Job summary

AbbVie is seeking a Central Monitoring Manager I in New Jersey to lead a global team delivering high-quality central monitoring for clinical studies. You will drive strategic RBQM execution, collaborate with study teams, and guide staff through coaching, performance reviews, and cross-functional partnerships.

You will oversee staffing, budgeting, and process improvements while ensuring compliance with ICH/GCP and AbbVie policies.

Qualifications

  • Strong understanding of RBQM and risk-based monitoring in clinical trials.
  • Proven experience leading front-line teams and coordinating with cross-functional stakeholders.
  • Excellent communication to drive decisions and coach staff across geographies.

Responsibilities

  • Deliver best-in-class central monitoring while driving cost efficiencies.
  • Partner with study teams to implement aggressive execution strategies.
  • Line manage Central Monitors: staffing, development, contracting, budgeting, hiring, reviews.
  • Advise and influence Clinical Site Management and cross-functional teams to strengthen RBQM.
  • Support RBQM systems development for near real-time data analysis and quality.
  • Champion RBQM across AbbVie, aligning with multi-TA portfolios and development phases.
  • Ensure compliance with corporate/divisional policies and global regulations.

Skills

RBQM knowledge
People management
Global collaboration
Clinical trials

Education

Bachelor's degree in related field

Tools

Microsoft Office

Job description

AbbVie is seeking a Central Monitoring Manager I in New Jersey to lead a global team delivering high-quality central monitoring for clinical studies. You will drive strategic RBQM execution, collaborate with study teams, and guide staff through coaching, performance reviews, and cross-functional partnerships.

You will oversee staffing, budgeting, and process improvements while ensuring compliance with ICH/GCP and AbbVie policies.

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