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Risk Management Lead — Clinical Trials (Hybrid)

AbbVie · North Chicago, IL · Clinical Operations — Risk-Based Quality Management

Employment type

Full-time

Work setting

On-site

Location

North Chicago, IL

Schedule

Day shift

Posted

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Job overview

The Risk Management Lead — Clinical Trials role is hybrid, with onsite work Tuesday through Thursday, and candidates must be local to Lake County, IL; Irvine, CA; or Florham Park, NJ. Compensation is not specified. The role supports AbbVie’s global clinical trials and its Risk-Based Quality Management model; AbbVie’s mission is to deliver medicines and solutions for serious health issues. The lead advances risk-based quality management across clinical studies by guiding risk planning, monitoring risk signals, and helping teams implement mitigation measures. This work supports high-quality study execution, regulatory compliance, and continuous improvement across therapeutic areas.

What you'll do

  • Lead adoption of the end-to-end RBQM model across clinical study teams
  • develop risk strategies with cross-functional leads
  • facilitate Risk Assessment and Mitigation Planning meetings and maintain documentation
  • guide teams in identifying critical data and processes, KRIs, controls, and response plans
  • analyze quality metrics and risk signals
  • monitor mitigation execution and issue trends
  • support inspection readiness, audit response, and regulatory compliance
  • contribute to process optimization and knowledge sharing.

What we're looking for

Skills & competencies
risk management lead
clinical trials
hybrid
abbvie
risk-based quality management
central monitoring
risk assessment
risk mitigation
key risk indicators
clinical operations
regulatory compliance
lake county il
irvine ca
florham park nj
Work arrangement
  • Weekend coverage required

Benefits & perks

  • Paid time off
  • medical, dental, and vision insurance
  • 401(k)
  • long-term incentive program eligibility.

Why this role

Requires a bachelor’s degree in life sciences, risk-based, or a related discipline; an advanced degree is preferred. Requires at least 10 years of clinical operations experience and expertise in risk management, RBQM, or quality management. Hybrid schedule requires onsite work Tuesday through Thursday.

About the employer

AbbVie is hiring for this role. Industry: Pharmaceutical Preparation Manufacturing. Sector: 32.

Additional details

Industry sector
32
Industry
Pharmaceutical Preparation Manufacturing
Occupation code
13-1111.00
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