Global Clinical Site Management Lead

AbbVie

North Chicago (IL)

On-site

USD 120,000 - 160,000

Full time

14 days+
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Benefits offered by this job

Paid time off
Health insurance
401(k)

Job summary

The SML at AbbVie provides direction and operational expertise for Clinical Site Management (CSM) integrity, quality, and timeliness of activities in assigned studies, potentially serving as global study strategy leader.

In a matrix environment, you will coordinate with site monitors, the study strategy leader, and the Clinical Study Team to ensure site activation, engagement, protocol adherence and closeout across multiple phases and therapeutic areas.

Qualifications

  • Bachelor’s Degree or equivalent in a medical or scientific field.
  • 5+ years of industry clinical research experience with 2+ years in monitoring or project management on a global study.
  • Experience in Phase II/III studies and multiple therapeutic areas is highly desired.
  • Demonstrates leadership and strong written and verbal communication skills; able to influence in a matrix environment.
  • Fluent in English; strong planning and organizational abilities.

Responsibilities

  • Drive study-level global or area-level CSM deliverables with timelines and resources.
  • Define and lead site monitoring strategy and Site Engagement Strategy.
  • Maintain study-level and area-level timelines across the study lifecycle and support milestone execution.
  • Oversee monitoring activities and ensure quality, risk mitigation, and TMF completeness.
  • Collaborate with country leaders and the Clinical Study Team to manage risks and study execution.

Skills

Communication skills
Leadership
Project management
Influence without authority

Education

Bachelor’s Degree or equivalent

Tools

Microsoft Word
Microsoft PowerPoint
Microsoft Excel
Microsoft OneNote

Job description

The SML at AbbVie provides direction and operational expertise for Clinical Site Management (CSM) integrity, quality, and timeliness of activities in assigned studies, potentially serving as global study strategy leader.

In a matrix environment, you will coordinate with site monitors, the study strategy leader, and the Clinical Study Team to ensure site activation, engagement, protocol adherence and closeout across multiple phases and therapeutic areas.

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