Strategic Safety Program Manager

AbbVie Inc.

North Chicago (IL)

On-site

USD 120,000 - 170,000

Full time

2 days ago
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Benefits offered by this job

Long-term incentive programs
Comprehensive benefits package
Paid time off

Job summary

AbbVie Inc. in North Chicago seeks a Clinical Sciences Product Office professional to lead safety-focused program management across therapeutic areas.

You will coordinate cross-functional teams, influence key stakeholders, and drive strategic initiatives ensuring patient safety and product effectiveness. The role emphasizes strong communication, facilitation, and project-management skills in a matrix global environment, with opportunities to shape safety decisions and engage with industry

Qualifications

  • 3+ years clinical or pharmaceutical industry experience (advanced degree preferred).
  • Experience in clinical operations management, clinical study management, drug development, risk management, and/or drug safety operations preferred.
  • At least 3 years hands-on project management experience in leading cross-functional projects within a global company.

Responsibilities

  • Shape PST strategic priorities and drive implementation with strong Therapeutic Area/regulatory knowledge.
  • Manage multiple Product Safety Teams across Therapeutic Areas; plan meetings and document minutes.
  • Support PST Lead in framing safety issues and guiding decision making.
  • Escalate safety issues to management and SRB; prepare SRB discussions.
  • Strengthen internal and external engagement, including publications and conferences.
  • Develop deliverables through productive working sessions and robust outputs.
  • Support inspections/audit activities and CAPAs/commitments.

Skills

Project management
Stakeholder management
Cross-functional collaboration
Communication skills
Influencing
Leadership
Facilitation
Matrix team experience

Education

BA/BS in nursing or pharmacy, biologic/medical science, or healthcare professional preferred

Job description

AbbVie Inc. in North Chicago seeks a Clinical Sciences Product Office professional to lead safety-focused program management across therapeutic areas.

You will coordinate cross-functional teams, influence key stakeholders, and drive strategic initiatives ensuring patient safety and product effectiveness. The role emphasizes strong communication, facilitation, and project-management skills in a matrix global environment, with opportunities to shape safety decisions and engage with industry

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